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Patent Searching and Data


Matches 901 - 950 out of 2,195

Document Document Title
JPH11228536A
To obtain a new monomer facilitating its copolymerization with an aliphatic cyclic olefin, and capable of affording a resin having physical properties withstanding developers and resolving adhesion problem. This new monomer is shown by t...  
JPH11509534A
(57) Summary compound 3* (2 and 2* ジクロロ *3, 3, 3* truffe ルオロ *1* ヒドロキ Cipro pill) *2 and 2* ジメチル * (R 1, 3R) * cyclopropane carboxylic acid, Sis *3*. 2, 2*ジクロロ*3, and 3 --3* truffe ルオロ *1* ヒ...  
JPH11228491A
To provide a method for separating a cis/trans isomer mixture of 2-fluorocyclopropanecarboxylic acid by which the mixture is separated with little HF generation, and an apparatus made of a general purpose material can be used. A cis/tran...  
JPH11217354A
To readily obtain the subject optically high-purity chrysanthemum- monocarboxylic acid, by using a hydrophobic organic solvent as a separating solvent. A process for reacting (A) (±)-trans-chrysanthemum- monocarboxylic acid or (±)-cis/...  
JP2927605B2  
JP2921862B2  
JPH11507022A
(57) Those use in the medical treatment of the obstacle which accompanies summary saturation and unsaturated fatty acid, catechin ガラート, those derivatives, the new anti-androgen compound containing the similar thing on composition...  
JPH11130723A
To obtain a new compound useful as a raw material for a polymer or a precursor thereof. This new compound is a compound of the formula (X is hydrogen or a ≥1C alkyl), e.g. methyl ester of dicyclohexyl-2,3,3',4'-tetracarboxylic acid. Th...  
JP2889056B2  
JP2889702B2  
JPH11504624A
(57) The substitution 1* phenyl pyrazole *3* カルボキシ amide shown by formula (I) for using it as a compound which has high affinity to a summary human neurotensin receptor is indicated.  
JPH11106360A
To obtain the subject new compound useful as a raw material for electroconductive polymers, photographic photo-sensitive materials, fluorescent materials, transparent resin coatings for organic glasses, optical materials for optical fibe...  
JP2873090B2  
JP2867257B2  
JPH1149720A
To industrially and advantageously produce the subject derivative useful as a raw material for medicines, electrophotographic photoreceptors, liquid crystal elements or the like by reacting a specific cyclohepta[b]furan-2-one derivative ...  
JP2856116B2  
JP11021271A
To obtain the subject new compound wherein the number of carbon atoms is increased so as to raise the glass-transition temperature of polyester. This compound is shown by the formula (R1 and R2 are each an 1-10C alkyl; R3 is H or a 1-10C...  
JPH01121271A
NEW MATERIAL:A 2-substituted cycloheptimidazole derivative expressed by formula I (R and A are H or lower alkyl; B is lower alkanoyl, thenoyl, nicotinoyl, lower alkylsulfonyl or 3-alkoxycarbonylpropyl; n is 0 or 1) or acid addition salt ...  
JPH111453A
To easily obtain the optically active isomer of the subject compound useful as an intermediate for medicines, agricultural chemicals, etc., in an excellent yield and in a good optical purity by optically resolving cis-2- fluorocyclopropa...  
JP2840899B2  
JPH10330347A
To obtain the subject compound capable of being widely used for fluorescent whitening of materials to be dyed such as a knit or woven fabric, especially made of cotton and polyamide or for the fluorescent whitening of paper by deaminatin...  
JPH10324659A
To obtain the subject compound useful as an intermediate for agricultural and horticultural chemicals and medicines by an alkali saponification of a 1-4C alkyl ester corresponding to the subject compound in alkalinity under a specific co...  
JPH10316612A
To produce the subject compound in high selectivity and yield by oxidizing a specific aldehyde in an organic solvent in the presence of a catalyst with oxygen or an oxygen-containing gas in no need of large amounts of chromium compound, ...  
JP2825534B2  
JPH10298135A
To obtain the subject new compound useful as a pharmaceutical composition for curing or preventing a neurological disease, or bacterial or viral infection in a mammal. A compound of formula I [R1 is NHC(O)R5, etc.; R2 to R4 are each H, f...  
JPH10511387A
(57) -- summary book invention is useful in the medical treatment and tumor necrosis factor (TNF) production prevention of allergic nature and an inflammatory disorder -- new -- it is related with a 1, 3, and 3* (3 substitution) cyclohex...  
JPH10279532A
To obtain the subject compounds with microbicidal activity useful to produce other microbicidally active cyclopentane derivatives by reacting specific compounds each other under heating in the presence of a polar solvent. The compound sh...  
JP2809620B2
To provide the subject new compound useful as an inert fluid. This compound is expressed by the formula I (Z is COOCH3, COOC2H5 or COOC2H4OCH3), e.g. dimethyl 1,3-perfluorocyclohexanedicarboxylate of the formula II. The objective compoun...  
JPH10510656A
(-- 57) summary -- the method of controlling the memory system (10) which can be constituted after manufacture, and this system to operate the optimal. This system is an array which consists of two or more memory cells arranged with the ...  
JP2807792B2  
JP2808322B2  
JPH10509959A
(57) It is pharmacological and the purpose of summary book invention is to offer the Asia acid derivative displayed by following general formula I and its salt permitted, or ester. センテラ Before the Asia acid extracted from horse m...  
JPH10245360A
To provide a production process for carbonyl compound that can recover the noble metal complex as a rhodium complex in no need of precipitation of the complex, after the reaction mixture tentatively is taken out from the reactor in order...  
JPH10237015A
To provide an epimerization method capable of obtaining a potassium trans-2- or 4-substituted cyclohexanecarboxylate having substantially 100% purity solely in a single process. This epimerization method is to obtain a potassium trans-2-...  
JPH10509146A
(57) Process of treating various physiological states using the medicine composite and these containing inhibitor of summary matrix metalaw protease, and these. Have a compound of the present invention and a general formula and (T) A*B*D...  
JPH10231268A
To produce a cyclopropylacetylene derivative useful as a synthetic intermediate of a benzoxazinone derivative, etc., having anti-HIV activities under a mild condition by an industrially advantageous production method. A compound of formu...  
JP2788657B2  
JPH10218836A
To produce malonic acid and an alkylmalonic acid in high yields without generating salts by bringing an aqueous mixture of an ester into contact with a specific acidic ion-exchanger, distilling away the alcohol produced at the time, remo...  
JP2780381B2  
JP2776787B2  
JPH10507166A
(57) The production method of the cyclopropane carboxylic acid by non-contact oxidization of cyclopropane カルボキシ aldehyde which uses molecule-like oxygen as a summary oxidizer is indicated. Moreover, the production method of the...  
JPH10506383A
(57) The compound, method, and composite for inducing the increase in sodium excretion to the summary mammals are offered. The method for isolating and compounding the increase compound in sodium excretion is also offered. The medical tr...  
JPH10158218A
To provide the subject new compound useful as an inert fluid. This compound is expressed by the formula I (Z is COOCH3, COOC2H5 or COOC2H4OCH3), e.g. dimethyl 1,3-perfluorocyclohexanedicarboxylate of the formula II. The objective compoun...  
JPH10152453A
To produce a new bicyclo[3.2.1]octane derivative used by oral administration, having effective squalene synthase inhibiting activities and useful for treatment of cholesterinemia, etc., by substituting C atom for O atom of a specific oct...  
JPH10505610A
(-- 57) summary -- to how by new composition to have been improved for manufacturing R (+) * 1, 2, 3, and 6* tetra-ヒドロ *4* phenyl *1 (3* phenyl *3* cyclohexene *1* イル) methyl pyridine, The method from which 5* oxo *3* phenyl cy...  
JP2734725B2  
JPH1080298A
To obtain the subject compound useful as an intermediate, etc., for medicines, agrochemicals, etc., in high selectivity by subjecting a 2-halo-2- fluorocyclopropanecarboxylic acid ester to asymmetric hydrolysis with an esterase having as...  
JP2730776B2  
JPH10503206A
Halogenated compounds are prepared by ring opening reactions of highly fluorinated cyclopropanes with chlorine, bromine, iodine, or mixtures thereof at temperatures over 100 DEG C. A novel compound, which is one type of compound produced...  
JPH1072402A
To provide a method for selectively and efficiently producing a fluorocycolopropane derivative suitable as a production intermediate for a compound useful for production of a medicine, etc., by directly introducing fluorine atom to the c...  

Matches 901 - 950 out of 2,195