| 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 | Antimicrobial N-chlorinated compositions | US12614347 | 2009-11-06 | US08278482B2 | 2012-10-02 | Rakesh K. Jain; Eddy Low; Charles Francavilla; Timothy P. Shiau; Satheesh K. Nair |
| The present application relates to N-chlorinated cationic compounds of Formula I or a salt thereof, and associated compositions and methods of use as antimicrobial agents. | ||||||
| 142 | Oxime ether derivative and fungicide for agricultural and horticultural use | US12746892 | 2008-12-11 | US08268755B2 | 2012-09-18 | Hironori Furukawa; Raito Kuwahara; Hiroyasu Hosokawa; Kazuya Shimizu |
| The present invention provides a novel oxime ether derivative represented by the following formula (I), or salt thereof, that can be industrially produced advantageously, and can function as a fungicide for agricultural and horticultural use that has reliable effects and can be used safely, and a fungicide for agricultural and horticultural use that contains at least one of these compounds as an active ingredient thereof. In addition, the present invention provides a novel ketone derivative that is a production intermediate of the oxime ether derivative. | ||||||
| 143 | Use of 4-[(4-thiazolyl)phenoxy]alkoxy-benzamidine derivatives for treatment of osteoporosis | US12689878 | 2010-01-19 | US08227496B2 | 2012-07-24 | Hong-Suk Suh; Jin Soo Lee; Pan-Soo Kim; Yun-Ha Hwang; Jei Man Ryu; Yong-Ho Chung; Eun-Joo Kim; Do-Hui Kim; Yong-Youp Park |
| A method of treating osteoporosis comprising administering to a subject a composition comprising a compound, 4-{5-[4-(5-isopropyl-2-methyl-1,3-thiazol-4-yl)phenoxy]pentoxy}-benzamidine or a salt thereof, is described. A method of inhibiting osteoclast activity and stimulating osteoblast activity in a subject also is described. | ||||||
| 144 | Process for the production of stable polymers | US11591779 | 2006-11-02 | US08110704B2 | 2012-02-07 | James Michael Barnes; Hartmut Nefzger; Erika Bauer; Stefan Penninger; Thomas Schultz; Heinrich Lutz; Horst Di Mews; Charles S. Gracik |
| Stable NCO prepolymers are produced from polyisocyanates having a melting point greater than 70° C., preferably, naphthalene diisocyanate, having advantageous physical properties. An important feature of the process of the present invention is the rapid cooling of the prepolymer. The process of the present invention may be carried out on a continuous or batch basis. The prepolymers of the present invention are particularly suitable for the production of cast polyurethane elastomers. | ||||||
| 145 | Phenylazo-acetoacetanilide derivatives with a polymerizable functional group and related compounds as monomers for preparing polymeric pigment dispersants for inkjet inks | US11995329 | 2006-07-04 | US07812113B2 | 2010-10-12 | Geert Deroover; Wojciech Jaunky; Lambertus Groenendaal; Johan Loccufier |
| A monomer with a chromophore group represented by Formula (I): wherein AR1 represents a substituted or unsubstituted aromatic group; AR2 represents a substituted or unsubstituted aromatic group or a substituted or unsubstituted alkyl group; and R represents a substituted or unsubstituted alkyl group, with the proviso that one of R, AR1, and AR2 has a substituent with a polymerizable functional group. The monomer can be advantageously used to prepare polymeric dispersants for pigment dispersion, especially inkjet inks. | ||||||
| 146 | Process for preparing isocyanates in the gas phase | US10969704 | 2004-10-20 | US07754915B2 | 2010-07-13 | Heiko Herold; Volker Michele; Werner König |
| A process for preparing isocyanates in the gas phase, in which the mixing of the reactants and thus the reaction conditions are significantly improved by means of hydrodynamic measures such as increasing the turbulence of the feed stream in the central nozzle. As a consequence, the necessary residence time in the reactor and thus the length of the reactor are reduced and the formation of polymeric by-products which lead to caking in the reactor and a shortening of the operating period of the reactors is avoided. | ||||||
| 147 | Ester Compound and Use Thereof | US12528528 | 2009-02-27 | US20100035985A1 | 2010-02-11 | Tatsuya Mori |
| An ester compound represented by the formula (1): wherein R represents a C1-C4 alkyl group or a C3-C4 alkenyl group, and A represents a single bond or an oxygen atom, has an excellent pest controlling efficacy, and it is useful as an active ingredient of a pest controlling agent. | ||||||
| 148 | Pharmaceutical/cosmetic compositions comprising novel ligands that activate RAR receptors | US11403916 | 2006-04-14 | US07439396B2 | 2008-10-21 | Thibaud Biadatti; Anne-Pascale Luzy |
| Novel ligand compounds that activate RAR receptors have the following structural formula (I): and are suited for formulation into pharmaceutical compositions useful in human or veterinary medicine, or, alternatively, into cosmetic compositions. | ||||||
| 149 | Multistage continuous preparation of cycloaliphatic diisocyanates | US11185776 | 2005-07-21 | US07371891B2 | 2008-05-13 | Stephan Kohlstruk; Manfred Kreczinski; Hans-Werner Michalczak |
| The invention relates to a multistage process for continuous and phosgene-free preparation of cycloaliphatic diisocyanates. | ||||||
| 150 | 5-azido-laevulinic acid, method for the production thereof and its use | US10250708 | 2002-01-08 | US07319164B2 | 2008-01-15 | Sven Aldenkortt |
| The present invention relates to 5-azido levulinic acid, a process for its preparation, its use. Using 5-azido levulinic acid as starting material for the synthesis of 5-amino levulinic acid hydrochloride it is possible to obtain the latter in good yield an in pharmaceutical acceptable quality. 5-Azido levuliniv acid is synthesized in that methyl 5-bromo levulinate and/or methyl 5-chloro levulinate is converted with aqueous hydrochloric acid and as a result of an incomplete bromine/chlorine exchange at the C-5-postion a mixture of 5-chloro levulinic acid and 5-bromo levulinic acid is obtained, and the obtained 5-chloro levulinic acid, a mixture of 5-chloro levulinic acid and 5-bromo levulinic acid and the pure 5-bromo levulinic acid is transferred into 5-azido levulinic acid by conversion with a nucleophilic azide. | ||||||
| 151 | Carbon nanotube structure, method of manufacturing the same, carbon nanotube transfer body, and liquid solution | US10768039 | 2004-02-02 | US20050127030A1 | 2005-06-16 | Miho Watanabe; Kazunori Anazawa; Chikara Manabe; Masaki Hirakata; Kentaro Kishi; Taishi Shigematsu; Takashi Isozaki; Hiroyuki Watanabe; Shigeki Ooma; Shinsuke Okada |
| Provided is a carbon nanotube structure of homogeneous characteristics which is composed of at least a carbon nanotube structure layer where plural carbon nanotubes are cross-linked to one another to form a mesh structure on a surface of a base body. Also provided is a method of manufacturing the carbon nanotube structure which includes: an application step of applying a liquid solution that contains carbon nanotubes having functional groups and an additive for forming chemical bonds between the functional groups to a surface of a base body; and a cross-linking step for forming a carbon nanotube structure layer that has a mesh structure composed of the plural carbon nanotubes that are cross-linked to one another by chemical bonds formed among the functional groups. | ||||||
| 152 | Benzocycloheptenes, process for their production, pharmaceutical preparations that contain the latter as well as their use for the production of pharmaceutical agents | US10238640 | 2002-09-11 | US06878750B2 | 2005-04-12 | Rolf Bohlmann; Jorg Kroll; Hermann Kuenzer; Christa Hegele-Hartung; Monika Lessl; Rosemarie Lichtner; Yukishige Nishino |
| This invention describes the new benzocycloheptenes of general formula I in which R1, R2 and SK have the meanings that are indicated in the description. The new compounds have selective estrogenic activity on bones and are suitable for the production of pharmaceutical agents, especially for prophylaxis and therapy of osteoporosis. | ||||||
| 153 | Modified chain aliphatic polyamine | US10739006 | 2003-12-19 | US20040171791A1 | 2004-09-02 | Masatoshi Echigo; Hisayuki Kuwahara; Takeshi Koyama |
| A modified chain aliphatic polyamine obtained by addition reaction of a chain aliphatic polyamine having a specific structure and an unsaturated hydrocarbon compound has a low viscosity and it provides, when used as a curing agent for epoxy resin, an epoxy resin composition which can provide an epoxy resin cured product having an excellent property. Further, a modified chain aliphatic polyamine composition obtained by addition reaction of a chain aliphatic polyamine having a specific structure and an unsaturated hydrocarbon compound followed by the removing step of unreacted chain aliphatic polyamine to reduce its amount less than 2% by weight provides, when used as a curing agent for epoxy resin, an epoxy resin composition which can provide an epoxy resin cured product having an excellent property. | ||||||
| 154 | Novel nitric oxide-releasing imidate and thioimidate diazeniumdiolates, compositions, uses thereof and method of making same | US10702849 | 2003-11-06 | US20040092484A1 | 2004-05-13 | Ernst V. Arnold; Larry K. Keefer; Joseph A. Hrabie |
| The invention provides NO- or NOnull-releasing imidate, thioimidate, and amide diazeniumdiolates, in which the N2O2null functional group is bonded to a carbon atom. The invention also provides compositions comprising such diazeniumdiolate compounds, and methods of using such compounds and compositions. The invention further provides a method of preparing NO- or NOnull-releasing imidate, thioimidate, and amide diazeniumdiolates. | ||||||
| 155 | Composition and method for catalysis using bentonites | US10264139 | 2002-10-03 | US20030069446A1 | 2003-04-10 | Mohammed Belbachir; Abdelhak Bensaoula |
| Maghnia or Mostaganem bentonites, are activated by contacting the Maghnia or Mostaganem bentonite with an acid solution of selected concentration and then drying the Maghnia or Mostaganem bentonite to form an activated bentonite catalyst. This activated bentonite catalyst may be used to polymerize a vinyl, acrylic, cyclic ether, aldehyde, lactone or olefin monomer. In a further embodiment, a perflourinated amine or diamine is synthesized by contacting a Maghnia or Mostaganem bentonite with an acid solution of selected concentration, drying the Maghnia or Mostaganem bentonite, and absorbing a secondary amine with the Maghnia or Mostaganem bentonite to form a perflouroamide iodide salt. The perflouramide idodide salt can then be extracted with a polar solvent and neutralized by the use of a basic solution. | ||||||
| 156 | Multimodal polymers by controlled radical polymerization in the presence of alkoxyamines | US09828476 | 2001-04-09 | US20020040117A1 | 2002-04-04 | Olivier Guerret; Sophie Robin; Yves Gnanou |
| For the preparation of a multimodal polymer at least one monomer is subjected to free radical polymerization in the presence of several alkoxyamines comprising the sequence of formula: 1 in which RL is a monovalent radical exhibiting a molar mass of greater than 15, A represents the core of the alkoxyamine and n is a non-zero integer, the alkoxyamines exhibiting different values of n. | ||||||
| 157 | O- or S- substituted tetrahydronaphthalene derivatives having retinoid and/or retinoid antagonist-like biological activity | US667664 | 1996-06-21 | US5741896A | 1998-04-21 | Vidyasagar Vuligonda; Min Teng; Richard L. Beard; Alan T. Johnson; Yuan Lin; Roshantha A. Chandraratna |
| Compounds of the formula ##STR1## where the symbols have the meaning described in the application, have retinoid-like or retinoid antagonist-like biological activity. | ||||||
| 158 | Process for the production of cellulose moulded bodies | US454320 | 1995-06-05 | US5628941A | 1997-05-13 | Wolfram Kalt; Heinrich Firgo; Johann Manner; Eduard Mulleder; Bruno Mangeng; Arnold Nigsch; Franz Schwenninger; Christoph Schrempf |
| The invention is concerned with a process for the production of cellulose moulded bodies. In this process, cellulose is first dissolved in an aqueous solution of a tertiary amine-oxide, in particular N-methylmorpholine-N-oxide (NMMO), to produce a mouldable cellulose solution. Second, the cellulose solution is molded and conducted into an aqueous precipitation bath, wherein the cellulose is precipitated, which produces a moulded body and a spent precipitation bath. Next, the spent precipitation bath is regenerated. This regenerated aqueous amine-oxide solution is re-used to dissolve cellulose, thereby repeating the process. In the above process, the repeated aqueous amine-oxide solution has a pH within certain defined limits. | ||||||
| 159 | Novel insecticidal dibenzoyl-tert-butylcarbazonitrile compounds and method for the preparation thereof | US237346 | 1988-08-29 | US4857550A | 1989-08-15 | Vekataraman Kameswaran; Donald P. Wright, Jr.; Rod A. Herman |
| The present invention provides novel insecticidal dibenzoyl-tert-butylcarbazonitrile compounds and a method for the preparation thereof. It also provides methods for controlling insects with said dibenzoyl-tert-butylcarbazonitrile compounds and for protecting growing plants, crops, trees, shrubs and ornamentals, from attack by said insects. | ||||||
| 160 | Novel materials containing nitrogen | US327839 | 1973-01-30 | US3965184A | 1976-06-22 | Ronald Eric Banks; Robert Neville Haszeldine |
| Compositions of matter including the structural unit ##EQU1## wherein R.sub. F ' is a divalent polyfluoroalkylene group having a chain length of from 1 to 4 carbon atoms which may be substituted at one or more positions with chloro-or polyfluoroalkyl, chlorofluoroalkyl or polyfluorocycloalkyl groups containing up to six carbon atoms; and R.sub.F is a monovalent straight or branched chain, or cyclic, polyfluoroalkyl group or a chlorofluoroalkyl group containing up to ten carbon atoms and the R.sub.F groups are the same or different or is a divalent polyfluoroalkylene group having a chain length of from 1 to 4 carbon atoms which may be substituted at one or more positions with chloro or polyfluoroalkyl, chlorofluoroalkyl or polyfluorocycloalkyl groups containing up to six carbon atoms and the R.sub.F groups are interconnected to form a cyclic structure. | ||||||
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