Cas 15374-92-2,Acetic acid (13S,17S)-3-acetoxy-17-ethynyl-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-17-yl ester

15374-92-2

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Basic information

Product Name: Acetic acid (13S,17S)-3-acetoxy-17-ethynyl-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-17-yl ester
Synonyms:
CAS NO:15374-92-2
Molecular Formula:
Molecular Weight: 380.484
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Acetic acid (13S,17S)-3-acetoxy-17-ethynyl-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-17-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (13S,17S)-3-acetoxy-17-ethynyl-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-17-yl ester(15374-92-2)
EPA Substance Registry System: Acetic acid (13S,17S)-3-acetoxy-17-ethynyl-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-17-yl ester(15374-92-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 15374-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 15374-92-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,7 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15374-92:
(7*1)+(6*5)+(5*3)+(4*7)+(3*4)+(2*9)+(1*2)=112
112 % 10 = 2
So 15374-92-2 is a valid CAS Registry Number.

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15374-92-2Relevant academic research and scientific papers

17β-Ethynyl-3,17α-estradiol and derivatives thereof

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, (2008/06/13)

17β-ethynyl-3,17α-estradiol and derivatives thereof are prepared by epimerization of 17-acyl esters of 17α-ethynyl-3,17β-estradiol 3-ethers. 17α-ethynyl-3,17α-estradiol and its derivatives are active as post-coital antifertility agents and inhibit the growth of or reduce the size of the prostate gland and the seminal vesicle.

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