Benzoic acid (3S,8S,9S,10R,13R,14S,17R)-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

Base Information

Chemical Name:Benzoic acid (3S,8S,9S,10R,13R,14S,17R)-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
CAS No.:101047-07-8
Molecular Formula:C₄₃H₅₈O₄S
Molecular Weight:670.997
Hs Code.:

Benzoic acid (3S,8S,9S,10R,13R,14S,17R)-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

Synonyms:Benzoic acid (3S,8S,9S,10R,13R,14S,17R)-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

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Chemical Property of Benzoic acid (3S,8S,9S,10R,13R,14S,17R)-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

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Technology Process of Benzoic acid (3S,8S,9S,10R,13R,14S,17R)-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

There total 9 articles about Benzoic acid (3S,8S,9S,10R,13R,14S,17R)-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 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 101047-03-4,101143-33-3
24 (R/α)-isopropenylcholesterol benzoate

: 101047-07-8,112573-50-9,112573-51-0,112573-52-1,112573-53-2
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

Guidance literature:: Multi-step reaction with 3 steps

1: 10 mg / osmium tetroxide / diethyl ether; benzene / Ambient temperature

2: 1) aq. HIO₄; 2) NaBH₄ / 1)dioxane, 5 min ice-cooling; 2) MeOH, 30 min

3: 2.5 mg / pyridine / 14 h / Ambient temperature

With sodium tetrahydroborate; osmium(VIII) oxide; periodic acid; In pyridine; diethyl ether; benzene;

Reference yield:

: 101047-04-5,112515-97-6
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

: 101047-07-8,112573-50-9,112573-51-0,112573-52-1,112573-53-2
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

Guidance literature:: Multi-step reaction with 2 steps

1: 1) aq. HIO₄; 2) NaBH₄ / 1)dioxane, 5 min ice-cooling; 2) MeOH, 30 min

2: 2.5 mg / pyridine / 14 h / Ambient temperature

With sodium tetrahydroborate; periodic acid; In pyridine;

Reference yield:

: 101047-03-4,101143-33-3
24 (S/β)-isopropenylcholesterol benzoate

: 101047-07-8,112573-50-9,112573-51-0,112573-52-1,112573-53-2
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

Guidance literature:: Multi-step reaction with 3 steps

1: 7 mg / osmium tetroxide / diethyl ether; benzene / Ambient temperature

2: 1) aq. HIO₄; 2) NaBH₄ / 1) dioxane, ice-cooling, 5 min; 2) MeOH, 30 min

3: 2.5 mg / pyridine / 18 h / Ambient temperature

With sodium tetrahydroborate; osmium(VIII) oxide; periodic acid; In pyridine; diethyl ether; benzene;