Cas 845724-76-7,Acetic acid (3S,5S,8S,9S,10R,13S,14S,17S)-13-methyl-17-(2-methyl-[1,3]dioxolan-2-yl)-3-(toluene-4-sulfonyloxy)-hexadecahydro-cyclopenta[a]phenanthren-10-ylmethyl ester

845724-76-7

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Basic information

Product Name: Acetic acid (3S,5S,8S,9S,10R,13S,14S,17S)-13-methyl-17-(2-methyl-[1,3]dioxolan-2-yl)-3-(toluene-4-sulfonyloxy)-hexadecahydro-cyclopenta[a]phenanthren-10-ylmethyl ester
Synonyms:
CAS NO:845724-76-7
Molecular Formula:
Molecular Weight: 574.779
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 (3S,5S,8S,9S,10R,13S,14S,17S)-13-methyl-17-(2-methyl-[1,3]dioxolan-2-yl)-3-(toluene-4-sulfonyloxy)-hexadecahydro-cyclopenta[a]phenanthren-10-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (3S,5S,8S,9S,10R,13S,14S,17S)-13-methyl-17-(2-methyl-[1,3]dioxolan-2-yl)-3-(toluene-4-sulfonyloxy)-hexadecahydro-cyclopenta[a]phenanthren-10-ylmethyl ester(845724-76-7)
EPA Substance Registry System: Acetic acid (3S,5S,8S,9S,10R,13S,14S,17S)-13-methyl-17-(2-methyl-[1,3]dioxolan-2-yl)-3-(toluene-4-sulfonyloxy)-hexadecahydro-cyclopenta[a]phenanthren-10-ylmethyl ester(845724-76-7)

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: 845724-76-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 845724-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,5,7,2 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 845724-76:
(8*8)+(7*4)+(6*5)+(5*7)+(4*2)+(3*4)+(2*7)+(1*6)=197
197 % 10 = 7
So 845724-76-7 is a valid CAS Registry Number.

845724-76-7Upstream product

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845724-76-7Relevant academic research and scientific papers

Synthetic approach to 5α-pregnanolone 19-[O-(carboxymethyl)oxime] derivatives

Cerny, Ivan,Havlikova, Helena,Hill, Martin,Hampl, Richard,Pouzar, Vladimir

, p. 1805 - 1817 (2007/10/03)

Syntheses of 5α-pregnanolone derivatives (3-hydroxy-5α-pregnan- 20-ones) with 3α- and 3β-configuration and 19-[O-(carboxymethyl) oxime] group were developed, starting from 19-hydroxy-20-oxopregn-5-en-3β- yl acetate. After catalytic hydrogenation, acetylat

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