6035-63-8

Upstream product

• 481-14-1 isofucosterol 
• 98-88-4 benzoyl chloride 
• 101047-04-5 Benzoic acid (3S,8S,9S,10R,13R,14S)-17-((1R,4S)-5,6-dihydroxy-4-isopropyl-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 101047-04-5 Benzoic acid (3S,8S,9S,10R,13R,14S)-17-((1R,4R)-5,6-dihydroxy-4-isopropyl-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 101047-03-4 24 (R/α)-isopropenylcholesterol benzoate 
• 101047-03-4 24 (S/β)-isopropenylcholesterol benzoate 
• 101047-05-6 Benzoic acid (3S,8S,9S,10R,13R,14S)-17-((1R,4S)-5-hydroxy-4-isopropyl-1-methyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 101047-05-6 Benzoic acid (3S,8S,9S,10R,13R,14S)-17-((1R,4R)-5-hydroxy-4-isopropyl-1-methyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 101047-07-8 Benzoic acid (3S,8S,9S,10R,13R,14S)-17-((1R,4S)-4-isopropyl-1-methyl-5-phenoxythiocarbonyloxy-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 101047-07-8 Benzoic acid (3S,8S,9S,10R,13R,14S)-17-((1R,4R)-4-isopropyl-1-methyl-5-phenoxythiocarbonyloxy-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 481-14-1 Fucosterol 

Relevant academic research and scientific papers

STIGMASTA-5,24(28)-DIENE-3β-O-α-L-RHAMNOSIDE FROM CLEOME VISCOSA

Key Word Index: Cleome viscosa; Capparidiaceae; whole plant; new saponin; stigmasta-5,24(28)-diene-3β-O-α-L-rhamnoside.

Studies on the Constituents of Orchidaceous Plants. VII. The C-24 Stereochemistry of Cyclohomonervilol and 24-Isopropenylcholesterol, Non-conventional Side Chain Triterpene and Sterol, from Nervilia purpurea SCHLECHTER

The C-24 stereochemistry of cyclohomonervilol,a non-conventional side chain triterpene isoleted from Nervilia purpurea was determined to be 24S by chemical transformation to 24S-dihydrocyclofuntumienol.Separation of a 24-epimeric mixture of chemically syn