Cas 733047-17-1,Cyclobut[c]indene-2,5-diol, decahydro-2-methyl-, (2aS,4aR,5S,8aR)- (9CI)

733047-17-1

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Basic information

Product Name: Cyclobut[c]indene-2,5-diol, decahydro-2-methyl-, (2aS,4aR,5S,8aR)- (9CI)
Synonyms: Cyclobut[c]indene-2,5-diol, decahydro-2-methyl-, (2aS,4aR,5S,8aR)- (9CI)
CAS NO:733047-17-1
Molecular Formula: C12H20O2
Molecular Weight: 196.286
EINECS: N/A
Product Categories: CYCLOPENTANE
Mol File: 733047-17-1.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Cyclobut[c]indene-2,5-diol, decahydro-2-methyl-, (2aS,4aR,5S,8aR)- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Cyclobut[c]indene-2,5-diol, decahydro-2-methyl-, (2aS,4aR,5S,8aR)- (9CI)(733047-17-1)
EPA Substance Registry System: Cyclobut[c]indene-2,5-diol, decahydro-2-methyl-, (2aS,4aR,5S,8aR)- (9CI)(733047-17-1)

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: 733047-17-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 733047-17-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,3,0,4 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 733047-17:
(8*7)+(7*3)+(6*3)+(5*0)+(4*4)+(3*7)+(2*1)+(1*7)=141
141 % 10 = 1
So 733047-17-1 is a valid CAS Registry Number.

733047-17-1Upstream product

300344-51-8 1-((1S,3aR,4S,7aS)-4-Hydroxy-7a-methyl-octahydro-inden-1-yl)-ethanone

733047-17-1Downstream Products

733047-17-1Relevant academic research and scientific papers

Synthesis of novel analogues of 1α,25-dihydroxyvitamin D3 with side chains at C-18

Moman, Edelmiro,Nicoletti, Daniel,Mourino, Antonio

, p. 4615 - 4625 (2004)

Novel analogues of the hormone 1α,25-(OH)2-D3 with side chains attached to C-18 were synthesized by a versatile route in which key steps were the remote radical-induced functionalization of the 18-methyl by the C-8β-hydroxyl group an

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