专利汇可以提供Mono-5-substituted-thio-3-chloro-4H-1,2,6-thiadiazin-4-one antifungal agents专利检索,专利查询,专利分析的服务。并且Selected mono-5-substituted-thio-3-chloro-4H-1,2,6-thiadiazin-4-ones having the formula ##STR1## wherein X is substituted thio, are described which are useful for control of fungal disease in plants.,下面是Mono-5-substituted-thio-3-chloro-4H-1,2,6-thiadiazin-4-one antifungal agents专利的具体信息内容。
We claim:1. A method for control of fungal disease of plants comprising applying to the locus where control is desired an effective fungistatic or fungicidal amount of a compound having the formula: ##STR4## wherein X is alkylthio having 1 to 8 carbon atoms, phenylthio, phenyl (lower)-alkylthio, cycloalkylthio having 5 to 7 ring carbon atoms or substituted phenylthio having the formula: ##STR5## wherein each R is independently lower alkyl, lower alkoxyl, lower acylamino having 1 to 4 carbon atoms, lower alkoxycarbonyl, nitro, cyano or halogen and n is an integar having a value of 1 to 3 inclusive, with the proviso that when R is lower alkyl or halogen n maybe an integer having a value of 1 to 5 inclusive.2. The method of claim 1 wherein said compound is applied in admixture with an agriculturally acceptable carrier and a compatible surface active agent.3. The method of claim 2 wherein said compound is applied to seeds, plant foilage or soil in which plants are planted or are to be planted.4. An antifungal composition comprising an effective fungistatic or fungicidal amount of a compound of the formula: ##STR6## wherein X is alkylthio having 1 to 8 carbon atoms, phenylthio, phenyl (lower)-alkylthio, cycloalkylthio having 5 to 7 ring carbon atoms or substituted phenylthio having the formula: ##STR7## wherein each R is independently lower alkyl, lower alkoxyl, lower acylamino having 1 to 4 carbon atoms, lower alkoxycarbonyl, nitro, cyano or halogen and n is an integer having a value of 1 to 3 inclusive, with the proviso that when R is lower alkyl or halogen n may be an integer having a value of 1 to 5 inclusive, in admixture with an agriculturally acceptable carrier and a compatible surface active agent.5. The antifungal composition of claim 4 wherein X is other than methylthio or phenylthio.
BACKGROUND OF THE INVENTION
The present invention relates to a method for controlling fungal disease in plants, to novel antifungal compositions, and to compounds useful for controlling fungi which attack agricultural and garden plants and seeds. More particularly, the invention relates to the use of a selected mono-5-substituted-3-chloro-4H-1,2,6-thiadiazin-4-one as an antifungal agent for controlling fungal disease in plants.
Geevers and Trompen disclosed the preparation 3,5-dichloro-4H-1,2,6-thiadiazin-4-one and its use as an intermediate to prepare various other 5-substituted-3-chloro-4H-1,2,6-thiadiazin-4-ones including the 5-phenylthio and 5-methylthio derivative. J. Geevers and W. P. Trompen, Rec. Trav. Chim., 93, 270 (1974). The 5-phenoxy derivatives are disclosed in U.S. Patent Application Ser. No. 728,860 filed of even date herewith.
While the 5-phenylthio and 5-methylthio derivatives and the method for preparing them have been disclosed, the reference provides no indication of any biological activity. More particularly, there is no suggestion that the compounds of this invention have antifungal activity.
It has now been found that selected mono-5-substituted 3-chloro-4H-1,2,6-thiadiazin-4-ones, which are hereinafter described, exhibit excellent antifungal activity and are useful in providing control of fungal disease in agricultural crops by foliar, seed, and soil application.
SUMMARY OF THE INVENTION
The present invention thus provides (1) a method for controlling fungal disease in plants which comprises applying a selected mono-5-substituted-3-chloro-4H-1,2,6-thiadiazin-4-one, as defined below, to the locus where control is desired, (2) antifungal compositions for control of fungal disease in plants, and (3) certain novel compounds which are useful for control of fungi.
DETAILED DESCRIPTION
In accordance with a first aspect of the present invention, there is provided a method for controlling fungal disease in agricultural crops and other plants which comprises applying to the locus where control is desired an effective fungistatic or fungicidal amount of a mono-5-substituted-3-chloro-4H-1,2,6-thiadiazin-4-one of the formula ##STR2## in which X is alkylthio, phenylthio, phenyl(lower)alkylthio, cycloalkylthio having 5 to 7 ring carbon atoms or substituted phenylthio of the formula ##STR3## in which each R is independently selected from lower alkyl, lower alkoxyl, lower acylamino, lower alkoxycarbonyl, nitro, cyano or halogen and n is an integer having a value of 1-3. However, when R is lower alkyl or halogen n may have a value of 1 to 5 inclusive.
Unless it is otherwise indicated, the term "lower" means having 1 to 6 carbon atoms, straight or branched chain, preferably 1 to 4 carbon atoms, the term alkyl means having 1 to 8 carbon atoms, and the term "halogen" means bromine, chlorine and fluorine or iodine, advantageously bromine, chlorine or fluorine, preferably chlorine or bromine.
In the method of this invention an effective fungistatic or fungicidal amount of active ingredient is applied to foliage or seeds of agricultural plants or to the soil in which the plants are growing or are to be planted, i.e., the locus where control is desired. When so applied, the compounds prevent fungal infection or inhibit further development of a preexisting fungal disease.
In the method of this invention the selected antifungal agent may be applied as the technical material or as a formulated product. Typical formulations include the antifungal agent in combination with an agriculturally acceptable carrier, preferably with a surface active agent, and optionally with other active ingredients. Suitable formulations include granules, powders, or liquids, the choice varying with the fungus and environmental factors present at the particular locus of infestation. Thus the compounds may be formulated as granules of various sizes, as dusts, as wettable powders, as emulsifiable concentrates, as solutions, as dispersions, as controlled release compositions, and the like.
A typical formulation may vary widely in concentration of the active ingredient depending on the particular agent used, the additives and carriers used, other active ingredients, and the desired mode of application. With due consideration of these factors, the active ingredient of a typical formulation may, for example, be suitably present at a concentration of about 0.5% up to about 99.5% by weight of the formulation. Additives and carriers may comprise about 99.5% by weight to as low as about 0.5% by weight of the formulation. Surface active agents, if employed in the formulation, may be present at various concentrations, suitably in the range of 1% to 30% by weight.
The formulation may be used as such or diluted to a desired use dilution with a suitable diluent or carrier. The concentration of the active ingredient in use dilution is normally in the range of about 0.001% to about 4% by weight. Many variations of spraying, dusting, soil-incorporated, and controlled or slow release compositions in the art may be used by substituting or adding a compound of this invention into compositions known or apparent to the art.
The antifungal agents of this invention may be formulated and applied with other compatible active ingredients, including nematicides, insecticides, acaricides, other fungicides, plant regulators, herbicides, fertilizers, etc.
In applying the foregoing chemicals, whether alone or with other agricultural chemicals, an effective inhibitory or fungicidal amount of the active ingredient must be applied. While the application rate will vary widely depending on the choice of compound, the formulation and mode of application, the plant species being protected, and the planting density, a suitable use rate may be in the range of 0.05 to 5 kg/hectare, preferably 0.5 to about 4 kg/hectare.
The antifungal composition of this invention comprises a compound of formula I as defined above in admixture with an agriculturally acceptable carrier, preferably containing a compatible surface active agent.
The novel compounds of this invention are those of Formula I in which X is other than methylthio or phenylthio; that is, the compounds of formula I in which X is alkylthio of 2 to 8 carbon atoms, phenyl(lower)alkylthio, cycloalkylthio having 5-7 ring carbon atoms or substituted phenylthio of the Formula II in which R is lower alkyl, lower alkoxyl, lower acylamino, lower alkoxycarbonyl, nitro, cyano or halogen and n in an integer having a value of 1 to 3 inclusive, with the proviso that when R is lower alkyl or halogen n may have a value of 1 to 5 inclusive.
The compounds of this invention are prepared according to the teaching of Geevers and Trompen, supra; that is, by reaction 3,5-dichloro-4H-1,2,6-thiadiazin-4-one with thiolate ions, for example, sodium phenothiolate. The following examples are typical of the preparation of the compounds.
EXAMPLE I
Synthesis of 3,5-Dichloro-4H-1,2,6-thiadiazin-4-one
A 50 ml flask was charged with 20 ml formic acid. The flask was purged with a stream of dry nitrogen. The nitrogen purge was continued while 6.3 g 3,4,4,5-tetra-chloro-4H-1,2,6-thiadiazinone was added dropwise over 0.5 hour during which the temperature of the reaction mixture was maintained at 10±1° C. Following addition the reaction mixture was stirred at 10° C for 2 hours then at room temperature for 64 hours, then poured into 60 ml. ice-water with stirring. The resulting mixture was filtered and the filter cake washed with water and dried to yield 2.2 g of pale yellow 3,5-dichloro-4H-1,2,6-thiadiazin-4-one, mp 81°-82° C.
EXAMPLE II
Synthesis of 3-Chloro-5-phenylthio-4H-1,2,6-thiadiazin-4-one
In one portion 2.5 g of trimethylamine was added to a solution of 4.6 g of 3,5-dichloro-4H-1,2,6-thiadiazin-4-one in 75 ml of ethyl ether in a 250 ml flask. A solution of 2.8 g of thiophenol in 25 ml of ethyl ether was then added dropwise to the flask during a 15 minute period. The reaction was allowed to stir for 3 hrs. after which it was filtered. The filter cake was washed with ether, and the filter cake was discarded. Successively, the ether solution was washed twice with 50 ml of water and once with 50 ml of saturated sodium chloride solution. The ether solution was then dried over anhydrous sodium sulfate. The ether was evaporated, leaving a solid residue which was recrystallized from 75 ml of cyclohexane. The yellow-orange 3-chloro-5-phenylthio-4H-1,2,6-thiadiazin-4-one weighed 3.6 g, mp 99.5°-101.5° C. (Lit. mp 102.5°-103.5° C, J. Geevers and W. P. Trompen, supra.). The ir spectrum was consistent with the assigned structure.
Analyses calc'd for C9 H5 ClN2 OS2 : C 42.11; H 1.96; N 10.91. Found: C 42.39; H 2.07; N 10.94.
The compounds of this invention which are set forth below have been synthesized in accordance with the typical preparatory method set forth in Examples I and II. An identifying number is provided for each compound. This compound number is used below in reporting biological data realting to the compound.
______________________________________Compound No. Identity______________________________________1 3-chloro-5-(methylthio)- 4H-1,2,6-thiadiazin-4-one2 3-chloro-5-(ethylthio)- 4H-1,2,6-thiadiazin-4-one3 3-chloro-5-propylthio-4H- 1,2,6-thiadiazin-4-one4 5-butylthio-3-chloro-4H- 1,2,6-thiadiazin-4-one5 3-chloro-5-pentylthio-4H- 1,2,6-thiadiazin-4-one6 3-chloro-5-(phenylthio)- 4H-1,2,6-thiadiazin-4-one7 3-chloro-5-heptylthio-4H- 1,2,6-thiadiazin-4-one8 3-chloro-5-(phenylmethylthio)- 4H-1,2,6-thiadiazin-4-one9 3-chloro-5-(cyclohexylthio)- 4H-1,2,6-thiadiazin-4-one10 3-chloro-5-(4-methylphenylthio)- 4H-1,2,6-thiadiazin-4-one11 3-chloro-5-(4-methoxyphenylthio)- 4H-1,2,6-thiadiazin-4-one12 3-chloro-5-(4-chlorophenylthio)- 4H-1,2,6-thiadiazin-4-one13 3-chloro-5-(4-acetamido- phenylthio)-4H-1,2,6-thia- diazin-4-one14 3-chloro-5-(4-nitrophenylthio)- 4H-1,2,6-thiadiazin-4-one15 3-chloro-5-(2,4,5-trichloro- phenylthio)-4H-1,2,6-thiadiazin- 4-one______________________________________
The following examples demonstrate the practice of the present invention. The test organisms used in these examples, together with an identifying codes which are in the tables to identify each organism, are as follows:
As = alternaria solani
Bc = botrytis cinerea
Cc = cladosporium cucumerinum
Ep = erysiphe polygoni
Fs = fusarium solani
Ho = helminthosporium oryzae
Po = pyricularia oryzae
Pu = pythium ultimum
Rs = rhizoctonia solani
Sf = sclerotinia fructicola
Up = uromyces phaseoli
Pi = phytophthora infestans
Vi = venturia inaequalis
EXAMPLE III
Spore Germination Tests
The test chemical was dissolved or suspended in acetone in an amount such that 0.8 ml of the resulting suspension or solution, mixed with 40 ml water agar produced a water agar solution containing 40, 10, 2.5 and 1 ppm of test chemical. The resulting agar solution, at 50° C, was then divided equally between two sterile petri dishes, each having four separated quadrants, and allowed to solidify. Three quadrants of each dish were flooded with 0.1 ml of a spore suspension in sterile water. Spores of two pathogens, Erysiphe polygoni and Uromyes phaseoli, from infected plant leaves, were brushed on the remaining two quadrants. The tests were then incubated 48 hours, at 24° C.
Readings were then taken and the percentage of germinated spores calculated. From this percentage, a spore germination rating was assigned as follows:
______________________________________% Germination Rating______________________________________ 0 - 10 010 - 40 140 - 60 260 - 80 3 80 - 100 4______________________________________
Table I reports the inhibitory effect of these test compounds on spore germination and demonstrates improvement over benomyl which was used as a standard for comparison. In Table I, the lower the numeral used as a rating, the more effective the compound.
EXAMPLE IV
Mycelial Growth Tests
Aliquots of previously prepared solutions of active ingredient in acetone were added to tubes containing 20 ml of sterile, melted potato dextrose agar that had been cooled to 50° C to provide mixtures of 40, 20, 10, 5 and 2.5 ppm. The tubes were shaken to ensure thorough mixing of the chemical with the agar, and the mixture poured into petri dishes having 4 quadrants to solidify. Each quadrant was inoculated with a 4 mm diameter disc of agar containing mycelium of the test fungi and incubated at 25° C for 72-144 hours during which the samples were alternately exposed to light for 12 hours and to darkness for 12 hours. Growth was measured at the end of the incubation period by measuring the diameter of each fungus colony. Two measurements of the diameter, perpendicular to each other, were taken and the values averaged. Data are reported as percent inhibition (%I) by the following formula: ##EQU1## Captan and chlorothalonil were used as standards for comparison. The results reported in Table II indicate that the test compounds were generally more active than the standards.
EXAMPLE V
The compounds of this invention were tested for corp disease control to determine the basic types of antifungal activity they exhibit.
A. Foliar Protective Activity
The foliage of a tomato plant in the four leaf stage and a pinto bean in the primary leaf stage was sprayed with the test chemicals at a concentration of 150 ppm on a weight/volume basis, and the plant allowed to dry overnight.
Sporangia of Phytophthora infestans (late blight fungus) were harvested from cultures grown on lima bean agar for 10 to 14 days. A water suspension of sporangia (2 × 105 sporangia/ml) was incubated at 12° C for two hours in order to provide a zoospore suspension. Spores of Uromyces phaseoli (bean rust fungus) were collected from diseased plants and a 2% spore powder mixture prepared using ABB Pyrax talc as a diluent.
The tomato plants were inoculated in a spray hood with the zoospore suspension, then immediately incubated in a humidity chamber at 100% relative humidity at 18-20° C for four to five days. The bean plants were inoculated by dusting the spore powder onto the leaves. This was accomplished by placing the spore powder in a cheesecloth bag and shaking the bag over the leaves. The inoculated plants were placed in the humidity chamber at 100% relative humidity and 21° C for 24 hours and then placed in the greenhouse for four to six days until disease symptoms developed.
The percent disease control was then determined by comparing the disease incidence in treated plants and untreated check plants. Results reported in Table III demonstrate the efficacy of the compounds tested in preventing tomato late blight and bean rust when applied to foliage of uninfected plants at 150 ppm prior to disease infestation.
B. Foliar Curative Tests
In the curative tests the plants were inoculated with the appropriate pathogen 24 hours before chemical treatment. The following host-parasite combinations were used:
______________________________________PLANT FUNGUS DISEASE______________________________________Phaseolus vulgaris L. Uromyces phaseoli Link bean rustPhaseolus vulgaris L. Erysiphe polygoni DC bean powdery mildewBeta vulgaris Cercospora beticola sugar beet leaf spotOryzae sativa L. Pyricularia oryzae rice blast______________________________________
Spores of bean rust and bean powdery mildew were obtained from diseased plants. Spores of Cercospora beticola and Pyricularia oryzae were harvested from petri dish cultures. C. beticola was grown on potato dextrose agar and P. oryzae on a glucose yeast extract medium. The cultures were grown at 25° C for 10 days.
Beans (c. v. `Pinto`) were inoculated with rust as described in Example IV-A. Beans (c. v. `Bountiful`) at primary leaf stage were inoculated with powdery mildew by shaking diseased leaves over the test plants, thereby creating a spore deposit on leaves of the tests plants. Sugar beets and rice were inoculated by spraying a water suspension of spores of the appropriate pathogen on the foliage.
All of the plants except those inoculated with bean powdery mildew were incubated in the moisture chamber (21° C) for 24 hours. The bean powdery mildew inoculated plants were incubated in the greenhouse.
The test chemical was sprayed on the foliage of the plants at 150 ppm 24 hours after inoculation. The bean and rice plants were removed from the moisture chamber and allowed to dry before chemical treatment. After treatment the plants were incubated in the greenhouse for 6-10 days. The sugar beets were sprayed while still wet, after which they were immediately returned to the moisture chamber for two days and then to the greenhouse for 10-14 days.
The results tabulated in Table III demonstrate curative activity when the compounds were applied after infection of the plant.
C. Soil/Seed Treatment
Containers having a volume of about 0.25 l. were 2/3 filled with topsoil and 25 cucumber c.v. Straight Eight seeds deposited on the soil surface of each pot. A suspension containing 150 ppm of the test chemical was poured over the seeds and into the soil in sufficient quantity to provide 3.75 to 3.8 mg active ingredient per pot.
Fungi used in this test were Pythium ultimum and Rhizoctonia solani. These fungi were each grown on potato dextrose agar for three to six days. The agar plus mycelium was then minced in a blender with water and 10 ml of the resulting slurry of minced mycelium poured over the seeds.
Following inoculation approximately 15 mm of topsoil was spread over the seeds, the container capped and incubated at 4° C in darkness for three days, then transferred to a greenhouse (27° C) for 10-14 days, at which time stand counts were made. Captan was used as a standard for comparison. Based on stand counts an Efficacy Index was calculated for each test chemical as follows: ##EQU2##
The results, set forth in Table III, show that several of the compounds tested were considerably more effective than captan while others were less effective for cucumber damping-off complex.
In a similar manner the soil around a bean seedling was drenched with a sufficient amount of 150 ppm suspension of test chemical to provide 3.8 mg active per pot. Twenty-four hours later the soil was inoculated with a suspension of minced mycelium of Fusarium solani. The inoculated plants were then placed in a greenhouse, evaluated after fourteen days, and percent control of root rot damage calculated. The results, reported in Table III, indicate that only a few of the compounds were effective under the test conditions in treating bean root rot, but these provided a high degree of control.
TABLE I______________________________________Results of In Vitro Spore Germination Inhibition TestingCPD Conc. Spore Germination RatingNo. ppm BC PO VI AS CC PI EP UP______________________________________3 10 0 0 0 0 0 0 0 0 2.5 0 0 0 1 0 2 3 0 1.0 0 0 0 3 0 4 4 04 40 0 0 0 0 0 2 0 0 10 0 0 0 0 0 3 0 0 2.5 0 0 0 0 0 3 0 0 1.0 0 0 0 3 0 4 1 05 40 0 0 0 0 0 1 0 0 10 0 0 0 0 0 1 0 0 2.5 0 0 0 2 0 2 0 0 1.0 0 0 0 4 0 2 0 07 40 1* 0 0 1 0 0 0 0 10 2* 0 0 4 0 0 0 0 2.5 2 0 2 4 0 2 0 0 1.0 3 0 3 4 1 4 0 48 40 0 0 0 0 0 0 0 0 10 1* 0 0 3 0 0 0 0 2.5 1* 1 0 3 0 0 0 0 1.0 1* 0 0 3 0 0 1 09 40 0 0 0 0 0 0 0 0 10 0 0 0 1* 0 0 0 0 2.5 1* 0 0 3* 0 3 0 0 1.0 1* 0 0 4 0 4 2 010 10 0 0 0 0 0 0 0 0 2.5 0 0 0 1 0 0 0 0 1.0 0 0 0 4 0 0 0 011 40 0 0 0 0 0 0 0 0 10 0 1 0 0 0 0 1 0 2.5 0 0 0 3 0 2 3 0 1.0 0 2 0 4 0 4 4 112 40 0 0 0 0 0 0 0 0 10 0 0 1* 0 0 1 0 0 2.5 0 0 1* 0 0 1 0 0 1.0 0 0 1* 0 0 1 0 013 40 0 0 0 0 0 0 1 0 10 0 0 0 0 0 0 4 0 2.5 0 0 0 3 0 1 4 0 1.0 1 3 0 4 0 4 4 114 40 0 0 0 0 0 0 0 0 10 0 0 0 0 0 0 0 0 2.5 0 0 0 0 0 1 1 0 1.0 0 0 0 0 0 1 1 015 40 0 0 0 0 0 0 0 0 10 0 0 0 0 0 0 0 0 2.5 0 0 1* 0 0 1 0 0 1.0 0 0 1 3 0 1 1 1Benomyl 40 4* 0 0 4 0 1 0 0 10 4* 3* 0 4 3* 0 0 1* 1.0 4* 4* 3 4 4* 2 2 4______________________________________ *Abortive Germ Tubes
TABLE II__________________________________________________________________________Results of In Vitro Mycelial Growth Inhibition EvaluationPercent Fungus Growth InhibitorCPD Conc.No. ppm. AS FS SF PO PU RS HO CC__________________________________________________________________________1 40 -- 100 -- -- 100 100 100 -- 20 -- 100 -- -- 100 84 100 -- 10 -- 56 -- -- 24 64 77 -- 5 -- 93 -- -- 0 42 73 --2 40 -- 100 -- -- 100 100 100 -- 20 -- 100 -- -- 100 78 85 -- 10 -- 100 -- -- 38 56 73 -- 5 -- 81 -- -- 0 20 85 --3 40 100 100 100 100 100 100 100 100 20 90 100 100 93 100 100 100 71 10 81 100 100 63 100 89 89 42 5 81 42 100 30 60 73 74 334 40 35 100 100 100 100 100 100 100 20 87 100 100 47 100 100 100 54 10 55 63 100 40 100 87 89 42 5 48 74 100 20 84 82 79 335 40 61 79 100 47 100 87 89 54 20 48 47 100 33 100 84 100 50 10 68 74 88 30 89 84 79 25 5 55 58 100 13 69 64 58 336 40 -- 100 -- -- 100 82 100 -- 20 -- 100 -- -- 89 69 100 -- 10 -- 100 -- -- 0 42 50 -- 5 -- 100 -- -- 0 20 46 --7 40 16 58 39 13 49 64 68 29 20 29 58 33 13 0 33 58 33 10 16 58 21 13 0 31 49 13 5 16 37 21 13 0 38 21 138 40 48 33 47 23 0 47 41 8 20 24 5 23 29 0 0 24 0 10 24 14 20 3 0 0 18 17 5 0 24 20 3 0 0 6 09 40 55 79 55 30 100 80 100 42 20 35 74 88 20 89 87 79 38 10 39 63 100 30 64 64 78 42 5 48 -- 67 23 -- -- -- 3810 40 62 62 83 8 76 64 100 33 20 29 52 73 10 42 60 41 25 10 48 62 87 8 47 56 76 33 5 24 48 73 11 0 31 35 3311 40 77 100 100 73 100 78 100 63 20 55 74 100 93 100 78 100 67 10 48 84 94 50 100 82 58 42 5 45 42 76 53 100 69 68 1712 40 38 48 67 74 36 64 47 8 20 19 33 57 68 13 49 76 8 10 48 24 77 74 0 58 47 17 5 38 43 70 71 4 58 47 1713 40 86 52 90 94 100 69 88 8 20 81 48 90 90 78 56 65 8 10 57 33 87 52 52 73 53 17 5 43 29 67 58 51 46 41 014 40 24 29 40 65 16 53 17 33 20 24 24 63 45 0 24 41 0 10 0 23 53 48 0 22 65 0 5 0 24 50 35 0 20 18 015 40 57 48 67 65 87 69 76 25 20 52 71 60 61 100 78 100 17 10 5 52 50 61 100 67 100 8 5 0 48 23 39 76 69 100 0Captan 40 -- 44 -- -- 0 0 65 -- 20 -- 48 -- -- 0 0 62 -- 10 -- 33 -- -- 0 0 46 -- 5 -- 19 -- -- 0 0 18 --Chlor- 40 75 88 82 48 100 73 95 96thal- 20 38 76 76 41 100 53 73 71onil 10 50 41 70 15 31 40 59 63 5 44 41 67 26 0 31 50 63__________________________________________________________________________
TABLE III__________________________________________________________________________RESULTS OF FUNGICIDE PRIMARY SCREEN TESTING EfficacyPercent Disease Control IndexFoliar Curative Seed/Soil Sugar Cucumber Tomato Bean Beet Bean Damping-CPD Late Bean Bean Powdery Leaf Rice Root offNo. Blight Rust Rust Mildew Spot Blast Rot Complex__________________________________________________________________________1 0 0 0 50 0 0 0 1322 0 0 0 50 0 0 100 1263 0 0 0 0 0 0 0 994 0 0 0 0 0 0 0 1056 0 0 0 100 50 0 50 105 (a)7 0 0 0 0 0 0 0 08 100 0 0 90 95 0 0 010 98 0 0 0 0 0 0 011 0 90 0 0 0 0 0 8312 0 50 0 0 0 0 DP(b) 013 0 100 0 0 0 0 90 5314 95 100 0 0 0 0 0 7615 0 DP(b) 0 0 0 0 90 0__________________________________________________________________________ (a)Slight phylotoxicity (b)DP = Dead Plant
标题 | 发布/更新时间 | 阅读量 |
---|---|---|
植物病原真菌孢子捕捉装置以及系统 | 2020-05-08 | 553 |
一种噁霉灵与精甲霜灵复合颗粒剂及其制备方法 | 2020-05-08 | 110 |
一种硝基胍类化合物及其制备与应用 | 2020-05-13 | 136 |
一种含吲哚酰肼的杀菌组合物 | 2020-05-11 | 44 |
解淀粉芽孢杆菌在防治植物真菌病害中的应用 | 2020-05-12 | 765 |
一种缓释性杀菌杀虫剂及其应用 | 2020-05-13 | 93 |
一种广谱植物源杀菌剂及其制备方法和应用 | 2020-05-08 | 230 |
一株链霉菌、抑菌药物及其应用 | 2020-05-13 | 95 |
一种高产抗真菌活性物质菌株的构建及其应用 | 2020-05-13 | 189 |
一种血叶兰真菌病害监报设备 | 2020-05-12 | 825 |
高效检索全球专利专利汇是专利免费检索,专利查询,专利分析-国家发明专利查询检索分析平台,是提供专利分析,专利查询,专利检索等数据服务功能的知识产权数据服务商。
我们的产品包含105个国家的1.26亿组数据,免费查、免费专利分析。
专利汇分析报告产品可以对行业情报数据进行梳理分析,涉及维度包括行业专利基本状况分析、地域分析、技术分析、发明人分析、申请人分析、专利权人分析、失效分析、核心专利分析、法律分析、研发重点分析、企业专利处境分析、技术处境分析、专利寿命分析、企业定位分析、引证分析等超过60个分析角度,系统通过AI智能系统对图表进行解读,只需1分钟,一键生成行业专利分析报告。