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JPS5683465A |
PURPOSE: To prevent the deterioration in quality, discoloration and smelling of an amine oxide useful for a degreasing agent, etc. with time, by adding a specific preventing agent against deterioration in quality to the amine oxide or a ...
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JPS5661349A |
PURPOSE: To prepare the titled compound useful as a surface active agent having low irritation to the skin, e.g. a kitchen detergent, rinse such as shampoo, perfumery, cosmetics, etc., economically, in an industrial scale, in high effici...
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JPS5612617B2 |
A chain terpene alcohol having the formula (I) (II) wherein R1 and R2 are the same or different and respectively represent hydrogen atom or a lower alkyl group is produced by oxidizing a chain unsaturated amine having the formula wherein...
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JPS5526126B2 |
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JPS5517020B2 |
2-AMinobenzylamines (I): (where Hal = Cl or Br; R1 = H, Cl or Br; R2 = cyclohexyl, hydroxycyclohexyl, morpholinocarbonylmethyl or isopropylaminocarbonylmethyl gp.; R3 = H or methyl and R4 = H, or, if R2 = isopropylaminocarbonylmethyl or ...
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JPS5557552A |
This invention relates to compounds having the formula: wherein R1 and R2 are selected from the group consisting of hydrogen, acyl, trifluoroacetyl, straight chained and branched alkyl groups with up to 6 carbon atoms, such alkyl groups ...
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JPS5549346A |
Alpha-isocyano-carboxylic acid amides of the formula (I) wherein R1 and R2 are identical or different and each represent hydrogen, alkyl, alkenyl, alkynyl or aralkyl; or R1 and R2 together represent alkylene; and R3 is hydrogen, alkyl, a...
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JPS558971B2 |
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JPS5531079A |
N-oxalyl-N-phenyl-aminoacid or ester thereof of the formula (I) in which: R1 represents hydrogen, alkyl or halogen, R2 represents hydrogen or alkyl, R3 represents hydrogen or alkyl, R4 represents hydrogen, alkyl or optionally substituted...
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JPS55376B2 |
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JPS5441567B2 |
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JPS5440531B2 |
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JPS5440530B2 |
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JPS54151949A |
The pharmaceutical compositions contain cis- and trans-N-(2-aminocyclopentyl)-N-acylanilides of the general formula and their pharmacologically acceptable acid addition salts. The substituents are defined in Claim 1. These pharmaceutical...
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JPS54128546A |
Compounds of the formula [wherein p is zero or one; Q is oxygen or sulphur; R is alkyl, cycloalkyl, vinyl, ethoxy or methoxymethyl. R1 is hydrogen, alkyl, dimethylaminoalkyl, aralkyl or alkenylmethyl; and Y and Z are each hydrogen, halog...
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JPS54122233A |
The invention relates to substituted phenylnitramines and derivatives with fungicidal properties, and to the use of these compounds for the control of fungi, for example for the protection of living plants from attack thereby. The fungic...
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JPS54106451A |
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JPS5479230A |
New salts of alpha -isocyanocarboxylic acid of the formula wherein R is alkyl or phenyl, R1 is hydrogen, alkyl or phenylalkyl or R and R1 together represent an alkylene chain with at least 2 carbon atoms, and R2 is an alkali metal ion ar...
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JPS5348197B2 |
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JPS53141243A |
Compounds having the formula and the pharmaceutically acceptable salts thereof, wherein R1 is alkanoyl; R2 is alkyl; R3 is alkylamino, dialkylamino, a 1-piperazinyl group, 4-aryl-1,2,3,6-tetrahydro-1-pyridinyl, or N-alkyl-N-(pyridinylalk...
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JPS53119841A |
PURPOSE: Phenylglyoxal derivatives of formula I, e.g. 2-benzyloxyphenylglyoxal hydrate.
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JPS53116339A |
2-AMinobenzylamines (I): (where Hal = Cl or Br; R1 = H, Cl or Br; R2 = cyclohexyl, hydroxycyclohexyl, morpholinocarbonylmethyl or isopropylaminocarbonylmethyl gp.; R3 = H or methyl and R4 = H, or, if R2 = isopropylaminocarbonylmethyl or ...
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JPS5336453B2 |
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JPS5336452B2 |
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JPS5315345A |
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JPS5246935B1 |
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JPS52133087A |
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JPS52100459A |
Novel steroids having the structure and the 1,2-dehydro derivatives thereof, wherein R1 is hydrogen, hydroxy, alkanoyloxy, fluorine, chlorine, or bromine; R2 is alkyl or aryl; R3 is alkyl, aryl, alkanoyl, aroyl, alkoxycarbonyl, or cyano;...
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JPS5228791B2 |
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JPS5227150B2 |
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JPS5231008A |
PURPOSE: Geraniol and nerol, useful as raw materials of perfumery components or pharmaceuticals, are prepared in high yield with a few-stages process from isoprene and sec-amines as starting materials.
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JPS5219612A |
PURPOSE: Linalool is prepared in high yield with a few-stages by alcoholating after reacting isoprene with N, N-dialkylamine, and then with a peroxide.
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JPS5219613A |
PURPOSE: The high purity title compound, useful as perfumery or its raw material, is prepared in high yield from N, N-dialkyl[3,7-dimethyl-2,6-octadienyl]-amine.
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JPS5212986A |
The complex (I) consists of factors A, B, C and D, and the tetra (2-4C) acyl esters of factor A. The individual factors are also claimed. Factor A and its esters are of formula (II) (R, all the same, are H, a acetyl, propionyl or butyryl...
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JPS5145588B2 |
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JPS51124698A |
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JPS5137838B1 |
1285388 Liquid crystal compositions; dyes and pigments MERCK PATENT GmbH 2 Nov 1970 [28 March 1970] 52048/70 Heading C4P [Also in Division C2] The invention comprises compounds of the formula where X is an azo or azoxy group, R is a stra...
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JPS5136257B1 |
1285388 Liquid crystal compositions; dyes and pigments MERCK PATENT GmbH 2 Nov 1970 [28 March 1970] 52048/70 Heading C4P [Also in Division C2] The invention comprises compounds of the formula where X is an azo or azoxy group, R is a stra...
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JPS5133103B1 |
Cpds. of formula (I): (where R is H or CONHR1; R1 is H, alkyl, hydroxyalkyl, alkoxyalkyl, phenoxyalkyl, cycloalkyl(alkyl), or bicycloalkyl(alkyl) with 0-3 alkyl gps. on the cycloalkyl rings, or aryl or aralkyl with 0-3 alkyl, alkoxy, CF3...
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JPS5124504B2 |
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JPS5134123A |
1520441 Di-(substituted alkyl)amino-benzenes CHEM PHARMAZ FABRIK DR HERMANN THIEMANN GmbH 11 July 1975 [16 July 1974] 29218/75 Heading C3H [Also in Division C2] Novel compounds I in which R1 is Y is N or N#O, each of X1 and X2 is H or C1...
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JPS5132505A |
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JPS5111737A |
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JPS514086A |
Disclosed is a new class of surface active agents having anti-corrosion and oil-repellent properties and which are N,N'-bis-aminoalkylamides of polyoxaperfluoroalkandioic acids, their quaternary ammonium salts, and the oxides of the amin...
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JPS50160229A |
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JPS50140418A |
Cyclo-olefins are converted in high yield to the corresponding chloro-nitroso dimers by dissolving the cyclo-olefin in liquid SO2 and contacting with NOCl while maintaining a substantially oxygen-free environment. Even higher yields are ...
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JPS50121257A |
Novel N-oxide derivatives of bis-basic tricyclic ethers, their preparation and use for the prevention and inhibition of virus infections.
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JPS50121258A |
Novel N,N-dioxide derivatives of bis-basic cyclic ketones, their preparation and use for the prevention and inhibition of virus infections.
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JPS50121245A |
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JPS5025465B1 |
1377959 α-Methyl DOPA and derivatives thereof TANABE SEIYAKU CO Ltd 14 Dec 1971 [29 Dec 1970] 58091/71 Heading C2C Novel α - methyl - α - isocyano - # - phenyl propionic acid and esters thereof of the general formula wherein R is an a...
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