Cas 82467-88-7,(4S,5S,8S,9S,10R,13S,14S,17R)-4-Benzoyl-17-((R)-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-one

82467-88-7

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Basic information

Product Name: (4S,5S,8S,9S,10R,13S,14S,17R)-4-Benzoyl-17-((R)-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-one
Synonyms: (4S,5S,8S,9S,10R,13S,14S,17R)-4-Benzoyl-17-((R)-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-one
CAS NO:82467-88-7
Molecular Formula:
Molecular Weight: 436.635
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: (4S,5S,8S,9S,10R,13S,14S,17R)-4-Benzoyl-17-((R)-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-one(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5S,8S,9S,10R,13S,14S,17R)-4-Benzoyl-17-((R)-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-one(82467-88-7)
EPA Substance Registry System: (4S,5S,8S,9S,10R,13S,14S,17R)-4-Benzoyl-17-((R)-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-one(82467-88-7)

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: 82467-88-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 82467-88-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,4,6 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82467-88:
(7*8)+(6*2)+(5*4)+(4*6)+(3*7)+(2*8)+(1*8)=157
157 % 10 = 7
So 82467-88-7 is a valid CAS Registry Number.

82467-88-7Upstream product

82467-88-7Downstream Products

74850-10-5 (5α, 20-R)-4-diazo-21-hydroxy-20-methyl pregnan-3-one

82467-88-7Relevant academic research and scientific papers

Synthesis of 3-keto-4-diazo-5-α-dihydrosteroids as potential irreversible inhibitors of steroid 5-α-reductase

Metcalf, Brian W.,Jund, Karin,Burkhart, Joseph P.

, p. 15 - 18 (2007/10/02)

3-Keto-4-diazo-5-α-dihydrosteroids are prepared using the Hendrickson diazo transfer reaction on the corresponding β-diketones, which are available from 3-ketoΔ-4-steroids via Li/NH3 reduction and acylation of the kinetic enolate.

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