Cas 41882-71-7,(3-Benzoyl-phenyl)-acetic acid (3R,5S,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester

41882-71-7

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Basic information

Product Name: (3-Benzoyl-phenyl)-acetic acid (3R,5S,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester
Synonyms:
CAS NO:41882-71-7
Molecular Formula:
Molecular Weight: 610.921
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: (3-Benzoyl-phenyl)-acetic acid (3R,5S,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3-Benzoyl-phenyl)-acetic acid (3R,5S,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester(41882-71-7)
EPA Substance Registry System: (3-Benzoyl-phenyl)-acetic acid (3R,5S,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester(41882-71-7)

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: 41882-71-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 41882-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,8 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 41882-71:
(7*4)+(6*1)+(5*8)+(4*8)+(3*2)+(2*7)+(1*1)=127
127 % 10 = 7
So 41882-71-7 is a valid CAS Registry Number.

41882-71-7Upstream product

132652-51-8 5α-cholestan-3α-yl-3(hydroxyphenylmethyl)phenyl acetate

41882-71-7Downstream Products

132652-51-8 5α-cholestan-3α-yl-3(hydroxyphenylmethyl)phenyl acetate

41882-71-7Relevant academic research and scientific papers

LONG-RANGE INTRAMOLECULAR FUNCTIONALIZATION BY ALKOXYL RADICALS; LONG-RANGE INTRAMOLECULAR DOUBLE FUNCTIONALIZATION OF RING C OF CHOLESTANE AND ANDROSTANE SKELETONS

Orito, Kazuhiko,Ohto, Masaru,Sugawara, Naoto,Suginome, Hiroshi

, p. 5921 - 5924 (1990)

A one-step double introduction of a carbon-carbon double bond and oxygen functions to ring C of 5α-steroid skeletons, based on a long-range intramolecular hydrogen abstraction by alkoxyl radicals generated from the esters of 5α-cholestan-3α-ol carrying a

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