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JPH06509069A |
The invention relates to methods for the treatment of central nervous system disorders, gastrointestinal disorders, drug abuse, angina, migraine, hypertension and depression by administering a pharmaceutical composition comprising an eff...
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JPH06273926A |
PURPOSE: To provide the reflection-preventive film material precise in dimensional accuracy and matching accuracy, simple and easy in the manufacturing process and good in productivity and reproducibility, free from any problem on enviro...
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JPH06271517A |
PURPOSE: To only to improve selectivity to a (meth)acrylic acid alkylaminoalkyl ester, but also to enable the decomposition of by-products into reaction-starting compounds and reduce the amount of wastes, when the objective compound is p...
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JPH06256271A |
PURPOSE: To suppress the formation of a by-product and selectively obtain a compound by recovering the by-product, formed and remaining in the transesterification of an acrylic or a methacfylic ester with an alkylamino- alcohol and reuti...
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JPH0669995B2 |
New ethanolamine benzoate compounds, which can be used as medicaments and which correspond to the formula: in which R is as defined in the description, in the racemic and enantiomeric forms. These new compounds and their physiologically ...
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JPH0669997B2 |
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JPH0669996B2 |
NEW MATERIAL:A compound expressed by formula I [R<1> and R<2> are cycloalkyl, phenyl or 2-thienyl; R<3> and R<4> are H, alkyl or linked and, together with N, form cycloalkyl; R<5> and R<6> are H, alkyl or linked and, together with N, for...
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JPH06247911A |
PURPOSE: To obtain a liquid crystal compound having physical and chemical stabilities, exhibiting SC* phase over a wide temperature range and large spontaneous polarization, developing ferroelectricity by itself or as a mixture of other ...
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JPH06247826A |
PURPOSE: To provide an excellent humectant which is composed of a specific carboxyl betaine having high moisture retention, and can sustain the excellent effects for a long time, when used in cosmetics and detergents. CONSTITUTION: This ...
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JPH0662521B2 |
A novel compound, 6-acetoxymethyl-2-naphthoylcholine halide, is very stable to nonenzymatic hydrolysis and react specifically with cholinesterase in serum. A UV method for determining cholinesterase activity in serum which uses the novel...
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JPH0662500B2 |
Novel antiallergic agents are described which are carboxy-substituted 3,5-di(tertiary-butyl)-4-hydroxybenzophenones. Pharmaceutical compositions containing and pharmacological methods for using such compounds are also described, as are s...
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JPH0662542B2 |
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JPH06219997A |
PURPOSE: To obtain the subject compound in high yield used as a raw material in various industries by selectively nitrating p-site of a substituted amino group by allowing a specific aniline derivative to react with a nitrating agent, th...
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JPH06211743A |
PURPOSE: To obtain new substd. benzoic acids which are potent inhibitors of phospholipase A2 and useful in the treatment of psoriasis, inflammatory enteric diseases, asthma, allergy, arthritis, dermatitis, gout, lung diseases, myocardial...
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JPH0653711B2 |
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JPH0651663B2 |
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JPH0651664B2 |
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JPH06505721A |
PCT No. PCT/EP92/00512 Sec. 371 Date Sep. 16, 1993 Sec. 102(e) Date Sep. 16, 1993 PCT Filed Mar. 7, 1992 PCT Pub. No. WO92/16493 PCT Pub. Date Oct. 1, 1992.Esters of citric acid or acetylcitric anhydride with compounds of at least 3 OH g...
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JPH06505485A |
Trifluorobutenoic acid, its methyl ester and a process of preparation thereof.
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JPH0645574B2 |
The invention relates to novel compounds of formula I: wherein the symbols have the significances given in the description, the synthesis thereof and to the use of compounds of formula I for the control of pests such as insects mites and...
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JPH0643369B2 |
1. Claims (for the Contracting States : BE, CH, DE, FR, GB, IT, LI, LU, NL, SE) In all possible isomeric forms, or in the form of a mixture of isomers, the compounds with the formula I see diagramm : EP0050534,P45,F2 in which the cyclopr...
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JPH06157438A |
PURPOSE: To use an auxiliary which is avoided a difficulty of a conventional technique, further usable in an industrial scale, practicable easily and utilizable immediately in industry. CONSTITUTION: The aminophenylacetate or aminophenyl...
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JPH0641410B2 |
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JPH0635459B2 |
Novel compounds, e.g., 5,7-dimethyl-N-(2,6-dichlorolphenyl)-1,2,4-triazolo[1,5-a]py
rimidine-2 -sulfonami de and their compositions and use in the control of weeds and in the suppression of nitrification of ammonium nitrogen in soil. Oth...
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JPH06503836A |
The reaction products of (1) anhydrides and/or poly-acids and (2) aminoalcohols or aminoalcohols/amides with long chain hydrocarbyl groups attached improve the low-temperature properties of distillate fuel when added thereto.
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JPH0627106B2 |
This invention provides a group of hydroxycycloal- kanephenoxyethylamine antidepressant derivatives of the following structural formula:in whichR, is hydrogen or alkyl of 1 to 6 carbon atoms;R2 is alkyl of 1 to 6 carbon atoms;R3 and R4 a...
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JPH0625147B2 |
A compound of the formula : wherein R<1> is lower alkyl optionally substituted with a substituent selected from the group consisting of acyl,hydroxy, lower alkoxy, aryl, lower alkylthio and a group of the formula : in which R<5> is hydro...
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JPH0693590A |
PURPOSE: To provide the subject intermediate that has a specific chemical structure and can readily and effectively prepare a specific sizing agent. CONSTITUTION: The objective intermediate has at least one anionic or acidic group which ...
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JPH0687804A |
PURPOSE: To obtain the aminoacrylates having a viscosity up to 3000 mPa.s which enables particularly rapid curing when treated by radiation and to prepare thereof. CONSTITUTION: Aminoacrylates having viscosity of 200 to 3000 mPa.s at 23Â...
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JPH0617339B2 |
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JPH0665167A |
PURPOSE: To prepare the subject compd. useful for collecting formaldehyde present in a fabric. CONSTITUTION: This tris(2-acetacetoxy ethyl)-amine is obtained by reacting 2,2,6-trimethyl-oxo-1,3-dioxane with triethanolamine.
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JPH0613462B2 |
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JPH0641447A |
PURPOSE: To prepare a compound having non-linear optical properties by esterifying a specified compound with a methacrylic acid or a functional derivative thereof or methacryloyl chloride. CONSTITUTION: The compound expressed by formula ...
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JPH0632768A |
PURPOSE: To obtain the subject compound as a raw material for cationic polymers to be used as flocculants, antistatic agents, soil modifiers or paper strengthening agents by reaction of an unsaturated tertiary amine with methyl chloride ...
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JPH0625122A |
PURPOSE: To provide a new aniline derivative capable of easily and selectively producing agricultural chemicals and useful as an agricultural chemical intermediate. CONSTITUTION: (5-Amino-2-chloro-4-fluorophenyl) ethyl carbonate of formu...
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JPH0625684A |
PURPOSE: To obtain a friction modifier which can give a lubricating oil composition excellent in storage and oxidation stability and not undergoing phase separation even when it is present in a concentrated state in conjunction with othe...
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JPH0616602A |
PURPOSE: To produce a quaternary ammonium carbonate ester which is useful as a bleaching precursor in detergent compositions without accompanying generation of hydrogen chloride byproducts. CONSTITUTION: A hydroxyl compound of formula I ...
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JPH0616574A |
PURPOSE: To efficiently obtain the subject compd. in high yield which is useful as an antioxidant, lubricant, hydraulic fluid or the like by reacting each a specified, carboxylic acid ester and an alcohol in the presence of a specified c...
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JPH0616597A |
PURPOSE: To easily obtain in high yield a new diphenoxybenzene derivative having excellent antineoplastic activity, thus useful as an antineoplastic agent, by condensing a 3,5-dihydroxyaniline derivative with two molecules of a halonitro...
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JPH06500340A |
PCT No. PCT/FR92/00317 Sec. 371 Date Jan. 14, 1993 Sec. 102(e) Date Jan. 14, 1993 PCT Filed Apr. 10, 1992 PCT Pub. No. WO92/20646 PCT Pub. Date Nov. 26, 1992.The invention relates to the field of organic chemistry and more particularly t...
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JPH06500124A |
The imidazopyridines of formula wherein Ar represents a radical of the formula Z represents a radical of the formula The compounds are seterotonergic 5-HT3 antagonists. As such they are useful for the treatment of humans and animals wher...
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JPH0587062B2 |
NEW MATERIAL:A compound expressed by formula I [R<1>, R<2>, R<4> and R<6> are H, alkyl, cycloalkyl, aryl, alarkyl, etc.; R<3> and R<5> are H or alkyl; A is formula II (R<4> is H, alkyl, aryl, etc.; Q is 0-5), formula III (R<8> is H, alky...
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JPH05310654A |
PURPOSE: To reduce the hydrolysis and side reaction, eliminate a washing step, obtain an inexpensive ester and prevent the pollution from being caused by carrying out the esterification of an amino-alcohol with methacrylic acid using a m...
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JPH05294864A |
PURPOSE: To obtain a new fullerene derivative useful as a cross-linking agent and/or a nucleous constituent of star polymers. CONSTITUTION: This compd. is a polysubstd. fullerene component having more than one substd. groups selected fro...
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JPH05507073A |
PCT No. PCT/EP91/00863 Sec. 371 Date Nov. 16, 1992 Sec. 102(e) Date Nov. 16, 1992 PCT Filed May 8, 1991 PCT Pub. No. WO91/17974 PCT Pub. Date Nov. 28, 1991.Quaternized esters having fabric-softening and hydrophilicizing properties are ob...
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JP5071581B2 |
A novel phenylethanolaminotetraline having lipolytic activity of formula I wherin X represents hydrogen, halogen, a trifluoromethyl or a lower alkyl group and R represents hydrogen, a lower alkyl group not substituted or substituted by a...
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JPH05255209A |
PURPOSE: To provide a new compound that improves corrosion resistance on metal surface by applying it to the surface and reduces deterioration due to oxidation. CONSTITUTION: This is a new compound of formula I (R is H, a substituted or ...
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JPH05239002A |
PURPOSE: To obtain a new tricyclic compound useful as an anti-histamine agent and an antiallergic agent having low side effects and excellent selectivity. CONSTITUTION: A tricyclic compound of formula I [X is CH=CH, CH2O, CH2CH2 or O; Y ...
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JPH0563462B2 |
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JPH0560454B2 |
PURPOSE:To produce an acrylic monomer in high quality and yield, by heating and refluxing an ester adduct under reduced pressure prior to the reaction to lower the water content of the adduct below a specific level, adding an amino compo...
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