81757-79-1

Basic information

• Product Name: 12-benzoyloxypodocarpa-8,11,13-trien-19-oic acid
• CAS NO: 81757-79-1
• Molecular Weight: 378.468
• Mol File: 81757-79-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 12-benzoyloxypodocarpa-8,11,13-trien-19-oic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 12-benzoyloxypodocarpa-8,11,13-trien-19-oic acid(81757-79-1)
• EPA Substance Registry System: 12-benzoyloxypodocarpa-8,11,13-trien-19-oic acid(81757-79-1)

Safety Data

• Hazardous Substances Data: 81757-79-1(Hazardous Substances Data)

Upstream product

• 5947-49-9 podocarpic acid 
• 93-97-0 benzoic acid anhydride 

Downstream Products

• 135521-48-1 3α-hydroxy-18-nor-5β-podocarpa-8,11,13-trien-12-yl benzoate 
• 135521-30-1 3-oxo-18-nor-5β-podocarpa-8,11,13-trien-12-yl benzoate 
• 81758-01-2 12-benzoyloxy-6α-bromo-7-oxopodocarpa-8,11,13-trien-19-oic acid 
• 81757-99-5 12-benzoyloxy-7β-hydroxypodocarpa-8,11,13-trien-6β,19-olactone 
• 81757-97-3 12-benzoyloxy-7-oxopodocarpa-8,11,13-trien-19,6β-olactone 
• 214137-22-1 Benzoic acid (4bS,8R,8aR)-4b,8-dimethyl-8-(pyridin-2-ylsulfanyl)-4b,5,6,7,8,8a,9,10-octahydro-phenanthren-3-yl ester 
• 135521-23-2 Benzoic acid (4bS,8aS)-4b-methyl-8-methylene-4b,5,6,7,8,8a,9,10-octahydro-phenanthren-3-yl ester 
• 135521-19-6 3-oxo-19-norpodocarpa-4,8,11,13-tetraen-12-yl benzoate 
• 135521-41-4 2-oxo-19-nor-5β-podocarpa-3,8,11,13-tetraen-12-yl benzoate 
• 135521-38-9 7-oxo-19-norpodocarpa-4⁽¹⁸⁾,8,11,13-tetraen-12-yl benzoate 
• 135521-40-3 2-oxo-19-norpodocarpa-3,8,11,13-tetraen-12-yl benzoate 
• 135521-39-0 19-norpodocarpa-4,8,11,13-tetraen-12-yl benzoate 
• 135521-18-5 12-benzyloxy-18-norpodocarpa-8,11,13-trien-4α-yl acetate 
• 135521-35-6 Benzoic acid (4bS,8aS)-4b,8-dimethyl-4b,5,6,8a,9,10-hexahydro-phenanthren-3-yl ester 

Relevant articles and documents

Chemistry of the Podocarpaceae. LIX Dimerization of a Favorski-Type Rearrangement Product

Ozonolysis of podocarpic acid (1) followed by reduction of the resulting hydroperoxide (16) gives a moderate yield of the keto diacid (6).Treatment of the derived 7α-bromo keto acid (10) with potassium carbonate in acetone effects a Favorski-type rearrang