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JPS5212154A |
Disclosed are monomers of the formula: WHEREIN R is +TR R' is hydrogen or methyl; R'' is alkyl of 1-10 carbon atoms; X and Y are independently selected from the group consisting of NO2, halogen, cyano and -CF3; Z is oxygen or dicyanometh...
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JPS5140041B1 |
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JPS51125060A |
1500063 2-Indolinone and fluorenone derivatives SANDOZ Ltd 16 June 1975 [19 June 1974 (2)] 25530/75 Heading C2C Novel 2-indolinone and fluorenone derivatives of the general formula wherein Het is a radical formed by removing a hydrogen a...
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JPS512468B1 |
1,269,081. Hypoglycaemic compositions. J. R. GEIGY A.G. 14 March, 1969 [14 March, 1968], No. 13512/69. Heading A5B. [Also in Division C2] Pharmaceutical preparations showing hypoglycaemic action contain as active ingredient compounds I (...
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JPS511719B1 |
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JPS511718B1 |
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JPS50111021A |
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JPS5020068B1 |
1,269,081. Hypoglycaemic compositions. J. R. GEIGY A.G. 14 March, 1969 [14 March, 1968], No. 13512/69. Heading A5B. [Also in Division C2] Pharmaceutical preparations showing hypoglycaemic action contain as active ingredient compounds I (...
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JPS5020071B1 |
1,269,081. Hypoglycaemic compositions. J. R. GEIGY A.G. 14 March, 1969 [14 March, 1968], No. 13512/69. Heading A5B. [Also in Division C2] Pharmaceutical preparations showing hypoglycaemic action contain as active ingredient compounds I (...
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JPS5020070B1 |
1,269,081. Hypoglycaemic compositions. J. R. GEIGY A.G. 14 March, 1969 [14 March, 1968], No. 13512/69. Heading A5B. [Also in Division C2] Pharmaceutical preparations showing hypoglycaemic action contain as active ingredient compounds I (...
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JPS5020067B1 |
1,269,081. Hypoglycaemic compositions. J. R. GEIGY A.G. 14 March, 1969 [14 March, 1968], No. 13512/69. Heading A5B. [Also in Division C2] Pharmaceutical preparations showing hypoglycaemic action contain as active ingredient compounds I (...
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JPS5020069B1 |
1,269,081. Hypoglycaemic compositions. J. R. GEIGY A.G. 14 March, 1969 [14 March, 1968], No. 13512/69. Heading A5B. [Also in Division C2] Pharmaceutical preparations showing hypoglycaemic action contain as active ingredient compounds I (...
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JPS5070351A |
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JPS5058233A |
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JPS5058028A |
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JPS5013280B1 |
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JPS5013279B1 |
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JPS5052035A |
A novel process for the synthesis of substituted propanolamines from N-substituted aziridines.
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JPS5011374B2 |
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JPS5047920A |
1457159 N-Haloketimines BAYER AG 30 July 1974 [31 July 1973 (3)] 33560/74 Heading C2C N-Haloketimines of general formula where R 1 and R 2 are each linear or branched alkyl, cycloalkyl or aralkyl or 1-12C atoms; which is optionally subst...
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JPS5010593B1 |
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JPS5040557A |
Aziridinecarboxylic acid esters are prepared by trans-esterification of aziridinecarboxylic acid methyl, ethyl or propyl esters in the presence of a high-boiling paraffin hydrocarbon and optionally of an amine.
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JPS49133360A |
Compounds are provided having the structure: R2 R4 ¦ ¦ Z¦ O-C-COOR1 ¦ Z2 ¦ R5 Z1 (R3)n1 AND TO SALTS OF SUCH COMPOUNDS. These compounds are useful as hypocholesteremic agents and anti-inflammatory agents.
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JPS49132234A |
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JPS49125312A |
The invention relates to a method of preparation of 2-aminobutanol from readily available raw materials. The method of this invention is based on the reaction between 1.2-epoxybutane or isomeric butylene halogenehydrines with ammonia. Th...
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JPS49116030A |
Novel thiocarbamylsulfenamides containing two secondary carbon atom configurations in the N'N' positions adjoining the sulfur atom nitrogen are useful as accelerators in the vulcanization of unsaturated polymers. The compounds are prepar...
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JPS4995957A |
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JPS4986359A |
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JPS4982612A |
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JPS4927858B1 |
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JPS4966631A |
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JPS4961333A |
1386940 Furfuryl and pyranylmethyl urea derivatives MOBIL OIL CORP 26 April 1973 [20 June 1972] 19871/73 Heading C2C The invention comprises urea derivatives of ormula where R is 2-furyl, 2-tetrahydrofuryl, 3,4- dihydro-2H-2-pyranyl or 2...
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JPS4959090A |
The invention concerns epoxides and alcohols of the structures and [Rf(CH2)nSCH2]2CHOH and various derivatives thereof useful in leather and textile treatment.
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JPS4956918A |
A complexing agent for metal ions, preferably alkaline earth metal ions, which has the general formula III Y ¦ HN-Z ¦¦ (III) HO-C---CH ¦¦ XOOCCOOX wherein Z is one of the groups -CR3R4-COOX ¦H ¦¦ HC---C-OH ¦¦ XOOCCOOX or R5 ¦ ...
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JPS4951255A |
5,6,7,8-Tetrahydronaphthalenes having the structure and the pharmaceutically acceptable salts thereof, are useful as blood pressure lowering agents. In the above formula R1 can be hydrogen or alkyl; R2 is alkyl; R3 and R4 can each be hyd...
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JPS4949933A |
Cpds of formula (I) starting material for herbicides) where X = NO2 or H; R1R2 are indep. -12C alkyl, or NR1R2=aziridine, azetidine or pyrrolidine, or R1 = H and R2=1-5C alkyl, 2-3C alkenyl, 3-5C cycloalkyl or Ph (opt. substd. by one Cl ...
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JPS4917256B1 |
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JPS4941333A |
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JPS4924945A |
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JPS499090B1 |
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JPS4920164A |
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JPS4918846A |
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JPS4914456A |
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JPS495349B1 |
Compds. (R1R2)C6H3-X-CH2-Y-CH2-Z-C6H3(R3R4) (where R1 is NH2, AlkylNH, AlkanoylNH, AlkanoylIN(Alkyl) or AlkylINHSO2; R2 is H or Halogen; R3 and R4 are H, OH, NH2, halogen, alkyl or Oalkyl, X is O or S; Y is CH2, CHOH, CHOOCalkyl, CHOSO2a...
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JPS495350B1 |
Compds. (R1R2)C6H3-X-CH2-Y-CH2-Z-C6H3(R3R4) (where R1 is NH2, AlkylNH, AlkanoylNH, AlkanoylIN(Alkyl) or AlkylINHSO2; R2 is H or Halogen; R3 and R4 are H, OH, NH2, halogen, alkyl or Oalkyl, X is O or S; Y is CH2, CHOH, CHOOCalkyl, CHOSO2a...
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JPS495348B1 |
Compds. (R1R2)C6H3-X-CH2-Y-CH2-Z-C6H3(R3R4) (where R1 is NH2, AlkylNH, AlkanoylNH, AlkanoylIN(Alkyl) or AlkylINHSO2; R2 is H or Halogen; R3 and R4 are H, OH, NH2, halogen, alkyl or Oalkyl, X is O or S; Y is CH2, CHOH, CHOOCalkyl, CHOSO2a...
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JPS4913316A |
Title cpds. are of formula I, where R1-R8 = H, opt. subst. alkyl, aryl, aralkyl or alkaryl, hal, pseudohal, NO2, NH2, CONH2, OH, CHO, CO2H or SO3H.
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JPS493517B1 |
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JPS49184B1 |
1,261,572. Imidazolidine derivatives; preparation thereof. J. R. GEIGY A.G. 14 March, 1969 [14 March, 1968 (4)], No. 13508/69. Heading C2C. Compounds I (including salts thereof) wherein R 1 signifies C 1-5 alkyl, or an optionally alkyl-s...
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JPS4843614B1 |
1,268,584. Herbicides containing dinitrophenylenediamines. UNITED STATES BORAX & CHEMICAL CORP. 1 April, 1970 [1 April, 1969; 10 Nov., 1969 (2)], No. 15533/ 70. Heading A5E. [Also in Division C2] A herbicidal composition contains as acti...
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