Cas 96685-48-2,[(3aR,4R,6aR)-1-Benzenesulfonyl-4-(1,5-dimethyl-hexyl)-3a-methyl-octahydro-pentalen-2-yl]-methanol

96685-48-2

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Basic information

Product Name: [(3aR,4R,6aR)-1-Benzenesulfonyl-4-(1,5-dimethyl-hexyl)-3a-methyl-octahydro-pentalen-2-yl]-methanol
Synonyms: [(3aR,4R,6aR)-1-Benzenesulfonyl-4-(1,5-dimethyl-hexyl)-3a-methyl-octahydro-pentalen-2-yl]-methanol
CAS NO:96685-48-2
Molecular Formula:
Molecular Weight: 406.63
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: [(3aR,4R,6aR)-1-Benzenesulfonyl-4-(1,5-dimethyl-hexyl)-3a-methyl-octahydro-pentalen-2-yl]-methanol(CAS DataBase Reference)
NIST Chemistry Reference: [(3aR,4R,6aR)-1-Benzenesulfonyl-4-(1,5-dimethyl-hexyl)-3a-methyl-octahydro-pentalen-2-yl]-methanol(96685-48-2)
EPA Substance Registry System: [(3aR,4R,6aR)-1-Benzenesulfonyl-4-(1,5-dimethyl-hexyl)-3a-methyl-octahydro-pentalen-2-yl]-methanol(96685-48-2)

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: 96685-48-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 96685-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,6,8 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96685-48:
(7*9)+(6*6)+(5*6)+(4*8)+(3*5)+(2*4)+(1*8)=192
192 % 10 = 2
So 96685-48-2 is a valid CAS Registry Number.

96685-48-2Upstream product

96685-48-2Downstream Products

96685-48-2Relevant academic research and scientific papers

A MODIFIED SYNTHESIS OF THE (+)-8α-PHENYLSULPHONYL-DES-AB-CHOLESTANE VIA AN INTRAMOLECULAR NUCLEOPHILIC ATTACK TO EPOXIDE - A TOTAL SYNTHESIS OF VITAMIN D3

Nemoto, Hideo,Kurobe, Hiroshi,Fukumoto, Keiichiro,Kametani, Tetsuji

, p. 567 - 569 (2007/10/02)

An intramolecular alkylation of the phenylsulphonyl epoxide (6), which was readily obtained from the alsehyde (5), gave a separable mixture of the alcohols (7a) and (8a).The alcohol (8a) was then dehydrated via the corresponding mesylate (8b) to afford th

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