Cas 511544-31-3,4-Cyclohexene-1,2-diol, 1,5-dimethyl-6-(trimethylsilyl)-, (1R,2R,6R)- (9CI)

511544-31-3

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Basic information

Product Name: 4-Cyclohexene-1,2-diol, 1,5-dimethyl-6-(trimethylsilyl)-, (1R,2R,6R)- (9CI)
Synonyms: 4-Cyclohexene-1,2-diol, 1,5-dimethyl-6-(trimethylsilyl)-, (1R,2R,6R)- (9CI)
CAS NO:511544-31-3
Molecular Formula: C11H22O2Si
Molecular Weight: 214.37668
EINECS: N/A
Product Categories: ALCOHOL
Mol File: 511544-31-3.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: 4-Cyclohexene-1,2-diol, 1,5-dimethyl-6-(trimethylsilyl)-, (1R,2R,6R)- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: 4-Cyclohexene-1,2-diol, 1,5-dimethyl-6-(trimethylsilyl)-, (1R,2R,6R)- (9CI)(511544-31-3)
EPA Substance Registry System: 4-Cyclohexene-1,2-diol, 1,5-dimethyl-6-(trimethylsilyl)-, (1R,2R,6R)- (9CI)(511544-31-3)

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: 511544-31-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 511544-31-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,1,5,4 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 511544-31:
(8*5)+(7*1)+(6*1)+(5*5)+(4*4)+(3*4)+(2*3)+(1*1)=113
113 % 10 = 3
So 511544-31-3 is a valid CAS Registry Number.

511544-31-3Upstream product

55861-03-5 (2,6-dimethylcyclohexa-2,5-dienyl)trimethylsilane

511544-31-3Downstream Products

511544-31-3Relevant academic research and scientific papers

Desymmetrization of cyclohexa-1,4-dienes - A straightforward route to cyclic and acyclic polyhydroxylated systems

Landais, Yannick,Zekri, Elisabeth

, p. 4037 - 4053 (2007/10/03)

A straightforward route to polyols, amino polyols, polysubstituted lactols and lactones from readily available arenes has been devised. It uses a three- or four-step sequence involving a Birch reduction of the arene, followed by desymmetrization through d

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