Document |
Document Title |
JPS6259694B2 |
Procedure for preparing new alkanolamine derivatives, of formula: ** (Formula) ** in which R3 and R4, which may be the same or different, each represent hydrogen or a hydroxy radical, provided that at least one of R3 and R4 is a hydroxy ...
|
JPS62286961A |
NEW MATERIAL:A compound of formula I (R1 is H, 1W6C alkyl, 1W6C alkoxy or nitro; R2 is 1W6C alkyl or 6W10C aromatic hydrocarbon group; R3 is R2, 1W6C alkoxy or 6W10C aryloxy). EXAMPLE: 1-Ethoxy-3-phenylpropanetrione 2-(O-ethoxycarbonyl)o...
|
JPS62283967A |
Compounds of Formula : in which n is 0 to 5, R is hydrogen or C1-4alkyl and X is hydrogen, halo, C1-4alkyl, CN, NO2, SO2NH2, COOH, CHO, OH, CH2OH, C1-4alkoxy, CF3, SO2CH3, SO2CF3 or CO2CaH2a+1 wherein a is 1 to 5 or any synthetically acc...
|
JPS62283956A |
NEW MATERIAL:A compound expressed by formula I (X is halogen; R is F- substituted 1W3C alkyl). EXAMPLE: N-(4-Bromo-2-fluoro-5-trifluoromethoxyphenyl)-N'-(2,6-difluo
robenzoyl) urea. USE: An insect pest controlling agent, having a wide in...
|
JPS6259102B2 |
|
JPS62281845A |
Compounds of formula I (wherein R represents a dec-1-(E)-enyl or dec-1-(Z)-enyl group in the m or p position), and salts thereof, inhibit 5-lipoxygenase product synthesis and are useful in the treatment of inflammatory, immuno-regulatory...
|
JPS6258346B2 |
|
JPS6257180B2 |
The reaction between L-aspartic acid and benzyloxycarbonyl chloride is carried out at a specific pH range, i.e., 12.0 to 13.5, whereby highly pure N-benzyloxycarbonyl-L-aspartic acid can be obtained in high yields, while both the by-prod...
|
JPS6257181B2 |
|
JPS62273944A |
NEW MATERIAL:A diacetylene compound of formula (n is 1W18). EXAMPLE: 2,4-Hexadiyne-1,6-dipentylurethane. USE: Useful as a functional material such as a non-linear optical material, memory material, electrically conductive material, etc. ...
|
JPS6256878B2 |
Tin-containing oxime derivatives of the formula wherein n is 0, 1 or 2, m is 0 or 1, Ar is an optionally substituted phenyl radical or an optionally substituted naphthyl radical or, when m is 0, Ar may also be an ester group, X is hydrog...
|
JPS6256864B2 |
New m-anilide-urethanes, processes for their manufacture, herbicides containing these compounds, and processes for controlling unwanted plant growth with these compounds.
|
JPS6256865B2 |
|
JPS6256144B2 |
|
JPS62267258A |
(57) [Abstract] Since this gazette is application data in front of an electronic application, the data of an abstract is not recorded.
|
JPS62267279A |
(57) [Abstract] Since this gazette is application data in front of an electronic application, the data of an abstract is not recorded.
|
JPS6254780B2 |
A fluorine-containing vinyl compound of the formula: (I) wherein Rf is fluoroalkyl of 4 to 20 carbon atoms, R1 is hydrogen or acyl of 1 to 3 carbon atoms, one of R2 and R3 is hydrogen and the other is methyl, R4 is hydrogen or methyl, A ...
|
JPS6254300B2 |
|
JPS6254302B2 |
|
JPS62502835A |
(57) [Abstract] Since this gazette is application data in front of an electronic application, the data of an abstract is not recorded.
|
JPS62258349A |
The invention relates to compounds of the formula in which R<1> is absent or is hydrogen, alkyl or acyl, A is a carboxylic acid radical or an amino acid radical, and B is an amino acid radical, and R<2>, R<3> and R<4> are as defined in t...
|
JPS6253510B2 |
|
JPS62258350A |
Substituted amino carbamate derivatives corresponding to the formula are effective in stabilizing organic materials against oxidative, thermal and actinic degradation, said derivatives being particularly effective as color improvers and ...
|
JPS62255455A |
Substituted aminoxy propionamide derivatives corrsponding to the formula said derivatives being useful as color improvers and stabilizers in various polymeric substrates.
|
JPS62252756A |
NEW MATERIAL:The compound of formula I [R1 is lower alkyl; R2 is hydroxyl, lower alkoxy, cycloalkyl, phenyl or (epoxy-substituted) alkyl, alkenyl or alkynyl; m is 0 or 1; n is 1 or 2]. EXAMPLE: p-Butylphenoxyacetaldehydeoxime o-propyl et...
|
JPS6251947B2 |
Salicylate ester-blocked polyisocyanates are of formula (Ie (where X is an organic gp. of valency n+m; R is H or 1-10C alkyl; R1 is 1-10C alkyl or 6-10C aryl; n is >=1; m is 0 or 1; m+n is >=2). Used for reaction with polybutadiene with ...
|
JPS62249945A |
PURPOSE: To obtain the titled compound useful as a production intermediate for pharmaceuticals, intermediate for organic compounds for photographic use, etc., under mild condition at a low cost in high yield, by reacting a hydroquinone d...
|
JPS6251264B2 |
|
JPS6251145B2 |
|
JPS62246548A |
(57) [Abstract] Since this gazette is application data in front of an electronic application, the data of an abstract is not recorded.
|
JPS6250460B2 |
|
JPS6250461B2 |
The invention relates to bis(nitrosoureido)-polyol derivatives of general formula I B1-A-B2 (I) wherein A stands for an open chain polyol comprising 4 to 6 carbon atoms or a six-membered cyclic polyol, and B1 and B2 being attached to two...
|
JPS62242653A |
PURPOSE: To obtain a compound useful as an intermediate for synthesizing proline, by reducing an N-substituted glutamic acid 5-ester with sodium boron hydride which is inexpensive, readily handleable, usable in an aqueous system has easy...
|
JPS62242656A |
Disclosed is a method of fighting fungus infections by using compounds having the general formula: wherein R is H, C1-C4 alkyl, alkenyl or alkynyl; n is 1 or 2; A represents a C1-C6 alkylene bridge, an arylene or a heterocyclic bridge; X...
|
JPS62240650A |
Substituted aminoxy propanoate derivatives corresponding to the formula are effective in stabilizing organic materials against oxidative, thermal and actinic degradation, said derivatives being particularly effective as color improvers a...
|
JPS62240648A |
(57) [Abstract] Since this gazette is application data in front of an electronic application, the data of an abstract is not recorded.
|
JPS62240656A |
The derivatives of the formula I in which R<1> is hydrogen, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-halogenoalkyl, halogen or nitro, R<2> is hydrogen, C1-C4-alkyl or C2-C4-alkenyl, R<3> is hydrogen, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-alkylthio, C...
|
JPS6249267B2 |
|
JPS62238256A |
PURPOSE: To obtain a modified isocyanate compound having excellent low- temperature storage stability and useful as a production raw material for polyurethane foam, by reacting an isocyanate with a compound having only one active hydroge...
|
JPS6249262B2 |
A process for the preparation of p-nitroso-diphenyl-hydroxylamines comprises the reaction of at least one nitroso compound of the benzene series in the present of a Lewis acid as catalyst in an amount of at least 0.5 mol per mol of nitro...
|
JPS62238257A |
Diarylguanidines can be isolated from the crude melt from the reaction of arylamines and cyanogen chloride in excellent quality and yield by dissolving the hot melt in water, extracting this solution with at least one polar, water-insolu...
|
JPS62238258A |
NEW MATERIAL:A compound of formula I [X is O or S; R1 is 1W3C alkyl; R2 and R3 are 1W3C alkyl or together form -(CH2)n; n is 3 or 4; R4 is 3W6C alkyl, alkenyl, (methyl-substituted) 5W7C cycloalkyl, etc.]. EXAMPLE: Isopropyl 2-(2-methoxy-...
|
JPS62502685A |
(57) [Abstract] Since this gazette is application data in front of an electronic application, the data of an abstract is not recorded.
|
JPS62234055A |
(57) [Abstract] Since this gazette is application data in front of an electronic application, the data of an abstract is not recorded.
|
JPS62234053A |
(57) [Abstract] Since this gazette is application data in front of an electronic application, the data of an abstract is not recorded.
|
JPS62230756A |
(57)【要約】 本公報は電子出願前の出願データであるため
要約のデータは記録されません。
|
JPS62230763A |
1. A process for the preparation of N,N-disubstituted mono- and oligourethanes, characterised in that N-mono- substituted mono- or oligo-urethanes corresponding to the general formulae I and II see diagramm : EP0238925,P9,F1 and see diag...
|
JPS62230762A |
NEW MATERIAL:A compound shown by formula I [R1 is H or methyl; Z is 2W8C bifinctional organic group; A is ring opening group of alkenylglyidyl ether shown by formula II (R3 is H or ≤20C halo-substituted hydrocarbon; R4 is 4h20C alkenyl...
|
JPS62230753A |
(57) [Abstract] Since this gazette is application data in front of an electronic application, the data of an abstract is not recorded.
|
JPS6247177B2 |
|