1258238-67-3

Basic information

• Product Name: ethyl (5β,8α,9β,10α,13α)-8-ethenyl-13-methyl-13-{(E)-[2-(4-nitrophenyl)hydrazinylidene]methyl}podocarpan-15-oate
• Synonyms: ethyl (5β,8α,9β,10α,13α)-8-ethenyl-13-methyl-13-{(E)-[2-(4-nitrophenyl)hydrazinylidene]methyl}podocarpan-15-oate
• CAS NO: 1258238-67-3
• Molecular Weight: 495.662
• Mol File: 1258238-67-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl (5β,8α,9β,10α,13α)-8-ethenyl-13-methyl-13-{(E)-[2-(4-nitrophenyl)hydrazinylidene]methyl}podocarpan-15-oate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (5β,8α,9β,10α,13α)-8-ethenyl-13-methyl-13-{(E)-[2-(4-nitrophenyl)hydrazinylidene]methyl}podocarpan-15-oate(1258238-67-3)
• EPA Substance Registry System: ethyl (5β,8α,9β,10α,13α)-8-ethenyl-13-methyl-13-{(E)-[2-(4-nitrophenyl)hydrazinylidene]methyl}podocarpan-15-oate(1258238-67-3)

Safety Data

• Hazardous Substances Data: 1258238-67-3(Hazardous Substances Data)

Upstream product

• 27975-19-5 isosteviol 
• 1149371-93-6 ethyl (5β,8α,9β,10α,13α)-8-ethenyl-13-formyl-13-methylpodocarpan-15-oate 
• 100-16-3 4-nitrophenylhydrazone 
• 1149371-92-5 ethyl (15β,16α)-16-hydroxy-15-({[(4-methylphenyl)sulfonyl]oxy}methyl)beyeran-18-oate 
• 160283-49-8 ethyl (4R,4aS,6aR,9S,11aR,11bS)-4,9,11b-trimethyl-8-oxotetradecahydro-6a,9-methanocyclohepta[a]naphthalene-4-carboxylate 
• 882175-41-9 ethyl (15β,16α)-16-hydroxy-15-(hydroxymethyl)beyeran-18-oate 

Downstream Products

• 1149372-05-3 ethyl (3S,6aR,6bS,8aS,9R,12aS,12bS)-1,3,5,6,6a,7,8,8a,9,10,11,12,12a,12b-tetradecahydro-3,9,12a-trimethyl-5-(4-nitrophenyl)-2H-3,6b-methanonaphtho[2',1': 3,4]cyclohepta[1,2-c]pyrazole-9-carboxylate 

Relevant articles and documents

Stereoselective synthesis, characterization, and antibacterial activities of novel isosteviol derivatives with D-ring modification

Considerable interests have been attracted by isosteviol and its derivatives because of their large variety of bioactivities. In this project, a series of novel 15- and 16-substituted isosteviol derivatives were stereoselectively prepared by means of func