728896-05-7

Basic information

• Product Name: 3-Vinyl-benzoic acid (2S,8S,8aR)-5-oxo-2-triisopropylsilanyloxy-1,2,3,5,8,8a-hexahydro-indolizin-8-yl ester
• Synonyms: 3-Vinyl-benzoic acid (2S,8S,8aR)-5-oxo-2-triisopropylsilanyloxy-1,2,3,5,8,8a-hexahydro-indolizin-8-yl ester
• CAS NO: 728896-05-7
• Molecular Weight: 455.67
• Mol File: 728896-05-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-Vinyl-benzoic acid (2S,8S,8aR)-5-oxo-2-triisopropylsilanyloxy-1,2,3,5,8,8a-hexahydro-indolizin-8-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Vinyl-benzoic acid (2S,8S,8aR)-5-oxo-2-triisopropylsilanyloxy-1,2,3,5,8,8a-hexahydro-indolizin-8-yl ester(728896-05-7)
• EPA Substance Registry System: 3-Vinyl-benzoic acid (2S,8S,8aR)-5-oxo-2-triisopropylsilanyloxy-1,2,3,5,8,8a-hexahydro-indolizin-8-yl ester(728896-05-7)

Safety Data

• Hazardous Substances Data: 728896-05-7(Hazardous Substances Data)

Upstream product

• 728895-62-3 (2R,4S)-2-(1-Acetoxy-allyl)-4-triisopropylsilanyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 728896-03-5 (2R,4S)-2-(1-Hydroxy-allyl)-4-triisopropylsilanyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 728895-66-7 Acetic acid 1-((2R,4S)-1-acryloyl-4-triisopropylsilanyloxy-pyrrolidin-2-yl)-allyl ester 
• 728896-00-2 (2R,4S)-2-Hydroxymethyl-4-triisopropylsilanyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 728895-69-0 Acetic acid (2S,8aR)-5-oxo-2-triisopropylsilanyloxy-1,2,3,5,8,8a-hexahydro-indolizin-8-yl ester 
• 728895-58-7 (2R,4S)-2-Formyl-4-triisopropylsilanyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 135042-17-0 (2R,4S)-1-tert-butyl 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate 
• 13154-24-0 triisopropylsilyl chloride 
• 28447-20-3 3-vinylbenzoic acid 
• 728895-73-6 (2S,8S,8aR)-8-Hydroxy-2-triisopropylsilanyloxy-2,3,8,8a-tetrahydro-1H-indolizin-5-one 

Downstream Products

• 728895-76-9 3-Vinyl-benzoic acid (2S,8S,8aR)-2-hydroxy-5-oxo-1,2,3,5,8,8a-hexahydro-indolizin-8-yl ester 

Relevant articles and documents

Design and synthesis of de novo cytotoxic alkaloids through mimicking taxoid skeleton

Based on a common pharmacophore model and the hypothesis that the baccatin core of taxoids is a scaffold securing the proper orientation of the side chains, a bicyclic alkaloid scaffold was designed as a baccatin surrogate. Using this scaffold, two novel