50611-92-2

Basic information

• Product Name: Benzoic acid (3S,8S,9S,10R,13R,14S)-17-(1,5-dimethyl-hexyl)-10,13-dimethyl-4-oxo-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester
• Synonyms: Benzoic acid (3S,8S,9S,10R,13R,14S)-17-(1,5-dimethyl-hexyl)-10,13-dimethyl-4-oxo-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester
• CAS NO: 50611-92-2
• Molecular Weight: 504.753
• Mol File: 50611-92-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzoic acid (3S,8S,9S,10R,13R,14S)-17-(1,5-dimethyl-hexyl)-10,13-dimethyl-4-oxo-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid (3S,8S,9S,10R,13R,14S)-17-(1,5-dimethyl-hexyl)-10,13-dimethyl-4-oxo-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester(50611-92-2)
• EPA Substance Registry System: Benzoic acid (3S,8S,9S,10R,13R,14S)-17-(1,5-dimethyl-hexyl)-10,13-dimethyl-4-oxo-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester(50611-92-2)

Safety Data

• Hazardous Substances Data: 50611-92-2(Hazardous Substances Data)

Upstream product

• 122441-58-1 3β-benzoylcholest-5-ene 
• 83685-71-6 3β-benzoyloxy-4β-hydroxy-5-cholestene 
• 604-32-0 cholesteryl benzoate 
• 83685-71-6 3β-benzoyloxycholest-5-en-4α-ol 

Downstream Products

• 34310-86-6 cholest-5-ene-3β,4β-diol 
• 83685-71-6 3β-benzoyloxycholest-5-en-4α-ol 
• 33444-61-0 5α-cholestane-3β,4β-diol 3-monobenzoate 
• 50611-95-5 <4α-2H>-cholest-5-ene-3β,4β-diol 3-benzoate 
• 83685-72-7 4-benzoyloxycholest-4-en-3-one 
• 83685-71-6 3β-benzoyloxy-4β-hydroxy-5-cholestene 
• 20834-98-4 5α-cholestane-3α,4α-diol 
• 50611-90-0 Benzoic acid (3S,4S,8S,9S,10R,13R,14S)-17-(1,5-dimethyl-hexyl)-4-hydroxy-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 

Relevant articles and documents

Catalytic allylic oxidation with a recyclable, fluorous seleninic acid

In conjunction with iodoxybenzene as reoxidant perfluorooctylseleninic acid catalyzes the allylic oxidation of alkenes to enones in trifluoromethylbenzene at reflux in moderate to good yield. After a reductive workup with sodium metabisulfite, the catalyst is recovered by fluorous extraction in the form of bis(perfluorooctyl) diselenide, which, itself, serves as a convenient catalyst precursor.

OXIDATION OF OLEFINS WITH 2-PYRIDINESELENINIC ANHYDRIDE

2-Pyridineseleninic anhydride, prepared in situ by oxidation of the corresponding diselenide with iodoxybenzene, is an efficient reagent for the conversion of olefins to unsaturated ketones with retention of the original position of the double bond.This r