Cas 610313-91-2,(R)-4-((5S,7R,8R,9S,10S,13R,14S,17R)-7-Methoxymethoxy-10,13-dimethyl-3-oxo-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentanal

610313-91-2

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Basic information

Product Name: (R)-4-((5S,7R,8R,9S,10S,13R,14S,17R)-7-Methoxymethoxy-10,13-dimethyl-3-oxo-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentanal
Synonyms: (R)-4-((5S,7R,8R,9S,10S,13R,14S,17R)-7-Methoxymethoxy-10,13-dimethyl-3-oxo-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentanal
CAS NO:610313-91-2
Molecular Formula:
Molecular Weight: 418.617
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: (R)-4-((5S,7R,8R,9S,10S,13R,14S,17R)-7-Methoxymethoxy-10,13-dimethyl-3-oxo-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentanal(CAS DataBase Reference)
NIST Chemistry Reference: (R)-4-((5S,7R,8R,9S,10S,13R,14S,17R)-7-Methoxymethoxy-10,13-dimethyl-3-oxo-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentanal(610313-91-2)
EPA Substance Registry System: (R)-4-((5S,7R,8R,9S,10S,13R,14S,17R)-7-Methoxymethoxy-10,13-dimethyl-3-oxo-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentanal(610313-91-2)

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: 610313-91-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 610313-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,0,3,1 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 610313-91:
(8*6)+(7*1)+(6*0)+(5*3)+(4*1)+(3*3)+(2*9)+(1*1)=102
102 % 10 = 2
So 610313-91-2 is a valid CAS Registry Number.

610313-91-2Upstream product

14773-00-3 methyl (5β,7α)-12-hydroxy-3-oxo-cholan-24-oate

610313-91-2Downstream Products

301695-61-4 (5α,7α,24R)-7,24-dihydroxy-3-ketocholestane

610313-91-2Relevant academic research and scientific papers

A concise and stereoselective synthesis of squalamine

Zhang, Dong-Hui,Cai, Feng,Zhou, Xiang-Dong,Zhou, Wei-Shan

, p. 3257 - 3259 (2007/10/03)

(Matrix presented) A short and highly stereoselective synthesis of the novel steroid squalamine (1) was accomplished in nine steps from easily available methyl chenodeoxylcholanate 2. Our synthesis featured improved dehydrogenation of 4 followed by conjugate reduction to construct the trans AB-ring system and efficient asymmetric isopropylation of aldehyde 6 to introduce the C-24R-hydroxyl group.

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