95119-02-1

Basic information

• Product Name: Acetic acid (3R,8R,9S,10S,13S,14S)-10,13-dimethyl-17-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester
• CAS NO: 95119-02-1
• Molecular Weight: 332.483
• Mol File: 95119-02-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Acetic acid (3R,8R,9S,10S,13S,14S)-10,13-dimethyl-17-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid (3R,8R,9S,10S,13S,14S)-10,13-dimethyl-17-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester(95119-02-1)
• EPA Substance Registry System: Acetic acid (3R,8R,9S,10S,13S,14S)-10,13-dimethyl-17-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester(95119-02-1)

Safety Data

• Hazardous Substances Data: 95119-02-1(Hazardous Substances Data)

Upstream product

• 17291-39-3 p-toluenesulfonate of 3β-acetoxy-5α-androstan-17β-ol 
• 1239-33-4 3β-acetoxy-13α-androsta-5,14-dien-17-one 
• 65694-40-8 (3β,5α)-3-acetyloxypregn-16-en-20-one oxime 

Downstream Products

• 1600-76-6 3β-acetoxy-5α-androstan-17α-ol 
• 2722-91-0 17α-amino-5α-androstan-3β-ol 
• 17291-39-3 p-toluenesulfonate of 3β-acetoxy-5α-androstan-17β-ol 
• 1600-76-6 Acetic acid (3R,8R,9S,10S,13S,14S,17S)-17-hydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester 
• 1600-76-6 3β-acetoxy-5α-androstan-17β-ol 
• 5615-34-9 17-hydroxyimino-5α-androstan-3β-ol 
• 23498-55-7 3β-acetoxy-17-hydroxyimine-5α-androstane 
• 2722-91-0 17β-amino-5α-androstan-3β-ol 

Relevant articles and documents

A new and concise way to enamides by fluoroalkanosulfonyl fluoride mediated Beckmann rearrangement of α,β-unsaturated ketoximes

The reaction of α,β-unsaturated ketoximes with fluoroalkanosulfonyl fluorides in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) underwent the Beckmann rearrangement smoothly to afford the corresponding acid-sensitive enamides in moderate to excellent yields, which provides a new efficient method for the preparation of acid-sensitive enamides.

Process for the preparation of 17β-hydroxy-3-oxo-17α-pregn-4-ene-21-carboxylic acid γ-lactone

A new process utilizing certain novel intermediates for the preparation of 17β-hydroxy-3-oxo-17α-pregn-4-ene-21-carboxylic acid γ-lactone is described herein. The procedure utilizes readily available and inexpensive sarsasaponin as starting material.

4-CHLOROSTEROIDS. SYNTHESIS OF 4-BETA-CHLORO-DEHYDROISOANDROSTERONE ACETATE AND OF 4-CHLORO-4-ANDROSTEN-3 BETA-OL-17-ONE ACETATE.

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