| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 141 | Novel oxime ethers, the preparation thereof, compositions containing them and the use thereof | US490055 | 1983-04-29 | US4566901A | 1986-01-28 | Henry Martin; Urs Fricker |
| The invention relates to novel oxime ethers of the formula I ##STR1## wherein R.sub.1 is hydrogen, halogen, lower alkyl, lower haloalkyl, lower alkoxy, lower haloalkoxy, lower alkylthio, lower haloalkylthio, lower alkylsulfinyl, lower alkylsulfonyl, lower haloalkylsulfinyl, lower haloalkylsulfonyl or nitro, each of R.sub.2 and R.sub.3 is hydrogen, halogen, lower alkyl, lower alkoxy or lower haloalkoxy, and Q is an unsubstituted or substituted lower alkyl, lower alkenyl, lower alkynyl or cycloalkyl group, a lower alkanoyl radical, an aliphatic, cycloaliphatic, aromatic or heterocyclic acyl radical which may be substituted or unsubstituted, a carbonyl or thiocarbonyl radical, an aryl or aralkyl radical, an acylimidomethyl radical, a phthalimidomethyl radical or a heterocyclic radical.These compounds are able to act as antidotes or safeners for protecting cultivated plants from the phytotoxic action of aggressive herbicides. Preferred crops are sorghum, cereals, maize and rice, and herbicides are chiefly chloroacetanilides and thiocarbamates. | ||||||
| 142 | Carbamate derivatives, insecticidal, miticidal or nematocidal compositions containing the same, and process for preparing the same | US352927 | 1982-02-26 | US4444786A | 1984-04-24 | Takeshi Goto; Hisashi Takao; Norio Yasudomi; Norio Osaki; Tadateru Murata |
| A novel S-methyl N-[{N-methyl-N-(N,N-disubstituted aminosulfenyl)carbamoyl}oxy]thioacetamidate derivative represented by the formula (I): ##STR1## which has insecticidal, miticidal or nematocidal activity comparable to or higher than known methomyl but which is quite low in toxicity to warm-blooded animals as compared to methomyl, is disclosed. An insecticidal, miticidal or nematocidal composition containing the same, and a process for preparing the same are also disclosed. A method for controlling noxious insects, mites or nematodes by using the same is further disclosed. | ||||||
| 143 | Stabilization of oxime carbamates with gallic acid, lower alkyl ester derivatives thereof | US323825 | 1981-11-23 | US4387053A | 1983-06-07 | James P. Glatzhofer |
| Stabilized pesticide compositions for use particularly as insecticides comprise gallic acid or the propyl ester thereof in combination with an oxime carbamate of the formula ##STR1## wherein R.sub.1 can be R.sub.2 -R.sub.4 or X; R.sub.2 -R.sub.4 can be H, lower alkyl, lower alkenyl, lower alkynyl, substituted alkyl, alkenyl or alkynyl with the proviso that R.sub.2 and R.sub.3 may be connected to form a cycloaliphatic ring;R.sub.5 can be R.sub.2 -R.sub.4 or X with the proviso that when R.sub.5 and X are OR.sub.8, SR.sub.8, S(O)R.sub.8, SO.sub.2 R.sub.8, or NR.sub.8 R.sub.9, R.sub.5 and X may be connected to form a heterocyclic ring;R.sub.6 -R.sub.7 can be hydrogen, lower alkyl, lower alkenyl or lower alkynyl;X=SR.sub.8, S(O)R.sub.8, SO.sub.2 R.sub.8, OR.sub.8, OSO.sub.2 R.sub.8, NR.sub.8 R.sub.9, NO.sub.2, CN, SCN, N.sub.3 or halogen; andR.sub.8 =H, lower alkyl, lower alkenyl lower alkynyl, aryl or substituted aryl, carbamyl, substituted carbamyl, acyl, or substituted acyl; and R.sub.9 =H or lower alkyl with the proviso that R.sub.8, R.sub.9 and N in the NR.sub.8 R.sub.9 group may form a heterocyclic ring. | ||||||
| 144 | Oximecarbamate derivatives, and their production and use | US317889 | 1981-11-03 | US4381935A | 1983-05-03 | Yoshiaki Kosuge; Ryo Yoshida; Seizo Sumida; Hirofumi Oshita; Soji Otsuki; Katsuzo Kamoshita |
| Oximecarbamate derivatives of the formula: ##STR1## wherein R.sub.1 is methyl or methoxy, R.sub.2 is lower alkyl, lower alkoxy, methylenedioxy, methylthio, halogen or trifluoromethyl, R.sub.3 is hydrogen, methyl or ethyl, X and Z are each oxygen or sulfur, m is an integer of 0 to 5 when R.sub.2 is fluorine or an integer of 0 to 3 when R.sub.2 is other than fluorine, R.sub.2 being same or different in case of m being an integer of 2 or 3, n and r are each an integer of 0 or 1 but when one of them is zero, the other is not zero, q is an integer of 0 or 1 and t is an integer of 0 to 4, which are useful as herbicides having high selectivity to crop plants. | ||||||
| 145 | 1-Chloro-1-p-methoxybenzoylformaldoxime-N-methylcarbamate | US171987 | 1980-07-24 | US4272453A | 1981-06-09 | David L. Booth; Joseph E. Gray |
| The compound 1-chloro-1-p-methoxybenzoylformaldoxime-N-methylcarbamate is useful as an antifungal agent. | ||||||
| 146 | N-Substituted alkyl-N-nitrosocarbamoyl azides | US22714 | 1979-03-21 | US4228086A | 1980-10-14 | Gerhard Eisenbrand |
| The invention relates to the preparation of novel N-substituted alkyl-N-nitrosocarbamoyl azides and to the compounds obtained thereby. The novel N-substituted alkyl-N-nitrosocarbamoyl azides can be reacted with amines, diamines, aminoalcohols, aminoacids or aminoacid derivatives to prepare unsymmetrically 1,3-disubstituted nitrosoureas which show therapeutical activity. | ||||||
| 147 | Butyramides and butyrates | US463987 | 1974-04-25 | US4059623A | 1977-11-22 | Russell Frank Bellina |
| Substituted 2-(carbamoyl)oxyimino-3-iminobutyramides and 2-(carbamoyl)oxyimino-3-iminobutyrates of the formula ##STR1## where Q is --OR.sub.4 or --NR.sub.5 R.sub.6, and A, R, R.sub.2, R.sub.3, R.sub.4, R.sub.5, and R.sub.6 are as hereinafter defined are useful as aphicides. The compounds are made by reacting an amine with a substituted 2-hydroxyiminoacetoacetamide (or 2-hydroxyiminopropionylacetamide) or an alkyl 2-hydroxyiminoacetoacetate (or 2-hydroxyiminopropionylacetate), then carbamylating the resulting substituted 2-hydroxyimino-3-iminobutyramide (or 2-hydroxyimino-3-iminovaleramide) or 2-hydroxyimino-3-iminobutyrate (or 2-hydroxyimino)-3-iminovalerate). | ||||||
| 148 | Carbamoyloximes derivatives | US483203 | 1974-06-26 | US3932509A | 1976-01-13 | Karl Gatzi |
| Carbamoyl oximes of the formula ##EQU1## their manufacture and fungicidal and virucidal activity are disclosed. In this formula R.sub.1 stand for alkylidene, aralkylidene or mono-, bi- or tricycloalkylidene and R.sub.2 stands for C.sub.8 to C.sub.14 alkyl, mono- or bicycloalkyl or cycloalkenyl. | ||||||
| 149 | AC Ketoxime carbamates | US22920772 | 1972-02-24 | US3875232A | 1975-04-01 | MAGEE THOMAS A |
| Carbamate derivatives of ketoximes are useful in combatting pests such as insects, mites, and nematodes.
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| 150 | Carbamoyl oximes | US12452771 | 1971-03-15 | US3843724A | 1974-10-22 | GATZI K |
| THEIR MANUFACTURE AND FUNGICIDAL AND VIRUCIDAL ACTIVITY ARE DISCLOSED. In this formula R1 stand for alkylidene, aralkylidene or mono-, bi- or tricycloalkylidene and R2 stands for C8 to C14 alkyl, mono- or bicycloalkyl or cycloalkenyl.
Carbamoyl oximes of the formula |
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| 151 | Carbamaldoximes | US40874473 | 1973-10-23 | US3836582A | 1974-09-17 | PERRONNET J; GIRAULT P |
| NOVEL CARBAMALDOXIMES OF THE FORMULA
X-C(-Y)=N-O-CO-NH-C(-CL)=C(-CL)2 WHERE Y IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, CHLORINE AND BROMINE AND X IS SELECTED FROM THE GROUP CONSISTING OF PHENYL OPTIONALLY SUBSTITUTED WITH AT LEAST ONE MEMBER OF THE GROUP CONSISTING OF HALOGEN CYANO-NO2, ALKYLL OF 1 TO 6 CARBON ATOMS AND ALKOXY OF 1 TO 6 CARBON ATOMS AND NITROFURYL HAVING FUNGICIDAL ACTIVITY. |
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| 152 | N-phenylthiocarbamoylthio-hydroximate pesticides | US18253771 | 1971-09-21 | US3825579A | 1974-07-23 | FUJIMOTO K; HIRANO M; TAKEDA H; OOBA S |
| A CARBAMATE COMPOUND OF THE FORMULA:
(R''-S-C(-R)=N-O-CO-N(-CH3)-S-),(X)N-BENZENE WHEREIN X IS HYDROGEN, LOWER ALKYL, LOWER ALKOXY, NITRO OR HALOGEN, R AND R'' ARE EACH LOWER ALKYL AND N IS AN INTEGER OF 1 TO 5, WHICH IS USEFUL AS AN INSECTICIDE, A NEMATOCIDE AND AN ACARICIDE WITH LESS TOXICITY TO WARMBLOODED ANIMALS AND CAN BE PREPARED BY REACTING A BENZENESULFENYL HALIDE OF THE FORMULA: (Z-S-),(X)N-BENZENE WHEREIN X AND N ARE EACH AS DEFINED ABOVE AND Z IS HALOGEN WITH AN N-METHYLCARBAMIC ESTER OF THE FORMULA: CH3-NH-CO-O-N=C(-R)-S-R'' WHEREIN R AND R'' ARE EACH AS DEFINED ABOVE IN AN INERT SOLVENT IN THE PRESENCE OF A BASE AT A TEMPERATURE OF -10 TO 50*C. |
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| 153 | Cycloalkane carboxaldoxime carbamates | US3721711D | 1970-04-29 | US3721711A | 1973-03-20 | MARAVETZ L |
| Chemical compounds useful as pesticides and characterized by the following structure: WHEREIN R1 is C1-C4 alkyl and R2, R3 and R4 are the same or different and are hydrogen or C1-C4 alkyl; n is 1 to 6 and m is 0, 1 or 2.
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| 154 | Carbamoyloximes | US3536760D | 1968-05-31 | US3536760A | 1970-10-27 | PAYNE LINWOOD K JR; WEIDEN MATHIAS H J |
| 155 | 2-methyl-2-nitrobicyclo(2.2.1)heptan-3-one n-methylcarbamoyloxime | US3479405D | 1968-05-31 | US3479405A | 1969-11-18 | PAYNE LINWOOD K JR; WEIDEN MATHIAS H J |
| 156 | Nitroalkyl carbamoyloximes | US39874464 | 1964-09-23 | US3400153A | 1968-09-03 | PAYNE JR LINWOOD K; WEIDEN MATHIAS H J |
| 157 | カルバモイルオキシム化合物並びに該化合物を含有する重合開始剤及び重合性組成物 | JP2020535773 | 2019-08-05 | JP7460288B2 | 2024-04-02 | 有吉 智幸; 大槻 竜也; 岡田 光裕 |
| 158 | カルバモイルオキシム化合物並びに該化合物を含有する重合開始剤及び重合性組成物 | JP2019030785 | 2019-08-05 | JPWO2020031986A1 | 2021-08-26 | 有吉 智幸; 大槻 竜也; 岡田 光裕 |
| 本発明の課題は、溶剤への溶解性が高く、且つ、満足できる感度(塩基発生能)を有する化合物、並びに、該化合物を重合開始剤として含有してなる重合性組成物及びその硬化物を提供することにある。本発明は、下記式(I)で表されるカルバモイルオキシム化合物を提供するものである。更に、本発明は、該化合物を含む重合開始剤、該重合開始剤及び重合性化合物を含有する重合性組成物、並びにその硬化物及びその製造方法を提供する。 式中の符号の定義は明細書を参照。 |
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| 159 | 殺有害生物的に活性なオキシムおよびヒドラゾン誘導体 | JP2017563077 | 2016-06-01 | JP2018525328A | 2018-09-06 | ベンファッティ フィデス; ジャンゲナ アンドレ |
| 本発明は、本明細書に定義される式(I) の化合物、これらの化合物を調製するための方法、これらの化合物を含む殺有害生物組成物、特に、殺虫、殺ダニ、殺軟体動物および殺線虫組成物、ならびに有害生物、例えば、昆虫、ダニ、軟体動物および線虫有害生物に対処しかつそれらを防除するためにこれらの組成物を使用する方法に関する。 |
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| 160 | 組成物、組成物の製造方法、不飽和化合物および不飽和化合物の製造方法 | JP2015029730 | 2015-02-18 | JP2016150922A | 2016-08-22 | 大野 勝俊; 森中 克利 |
| 【課題】不飽和化合物を製造する際に着色成分を生成する重合防止剤の添加量を削減できる、保管時の安定性および利用時の安定性に優れる組成物およびその製造方法を提供する。 【解決手段】不飽和イソシアネート化合物と、質量基準で0.01〜10ppmの三級アミン塩酸塩とを含有する組成物とする。組成物は質量基準で0.1ppm以上の三級アミン塩酸塩を含有するものであってもよい。不飽和イソシアネート化合物は、アクリロイルオキシエチルイソシアネートまたはメタクリロイルオキシエチルイソシアネートであることが好ましい。 【選択図】なし |
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