120632-49-7

Basic information

• Product Name: methyl (5Z)-7-((1R,2R,3S,5S)-2-(p-acetoxyphenyl sulfonylamino)-6,6-dimethylbicyclo<3.1.1>hept-3-yl)hept-5-enoates
• CAS NO: 120632-49-7
• Molecular Weight: 477.622
• Mol File: 120632-49-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl (5Z)-7-((1R,2R,3S,5S)-2-(p-acetoxyphenyl sulfonylamino)-6,6-dimethylbicyclo<3.1.1>hept-3-yl)hept-5-enoates(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (5Z)-7-((1R,2R,3S,5S)-2-(p-acetoxyphenyl sulfonylamino)-6,6-dimethylbicyclo<3.1.1>hept-3-yl)hept-5-enoates(120632-49-7)
• EPA Substance Registry System: methyl (5Z)-7-((1R,2R,3S,5S)-2-(p-acetoxyphenyl sulfonylamino)-6,6-dimethylbicyclo<3.1.1>hept-3-yl)hept-5-enoates(120632-49-7)

Safety Data

• Hazardous Substances Data: 120632-49-7(Hazardous Substances Data)

Upstream product

• 113158-27-3 (Z)-7-((1R,2R,3S,5S)-2-tert-Butoxycarbonylamino-6,6-dimethyl-bicyclo[3.1.1]hept-3-yl)-hept-5-enoic acid methyl ester 
• 113033-05-9 methyl (5Z)-7-((1S,2R,3S,5S)-2-carboxy-6,6-dimethylbicyclo<3.1.1>hept-3yl)-hept-5-enoate 
• 81806-60-2 (-)-methyl (5Z)-7-((1S,2R,3S,5S)-2-hydroxymethyl-6,6-dimethylbicyclo<3.1.1>hept-3-yl)hept-5-enoate 
• 86778-00-9 (+)-(4aR,6S,8S,8aR)-7,7-Dimethyl-6,8-methano-perhydroisochroman-3-ol 
• 126264-16-2 (+)-(5Z)-7-((1R,2R,3S,5S)-2-(tert-butoxycarbonylamino)-6,6-dimethylbicyclo<3.1.1>hept-3-yl)hept-5-enoic acid 
• 126264-15-1 [(1R,2R,3R,5S)-6,6-Dimethyl-3-(2-oxo-ethyl)-bicyclo[3.1.1]hept-2-yl]-carbamic acid tert-butyl ester 
• 126264-14-0 (+)-2-((1R,2R,3R,5S)-2-tert-butoxycarbonilamino-6,6-dimethylbicyclo<3.1.1>hept-3-yl)ethanol 
• 17814-85-6 (4-carboxybutyl)triphenylphosphonium bromide 
• 79119-26-9 4-acetoxybenzenesulfonyl chloride 
• 197069-37-7 (1R,2R,3S,5S)-(5Z)-7-(2-amino-6,6-dimethylbicyclo[3.1.1]hept-3-yl)-hept-5-enoic acid methyl ester 

Downstream Products

• 120632-66-8 (Z)-7-[(1R,2R,3S,5S)-2-(4-Hydroxy-benzenesulfonylamino)-6,6-dimethyl-bicyclo[3.1.1]hept-3-yl]-hept-5-enoic acid 

Relevant articles and documents

Thromboxane A2 receptor antagonists. III. Synthesis and pharmacological activity of 6,6-dimethylbicyclo[3.1.1]heptane derivatives with a substituted sulfonylamino group at C-2

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