Cas 127082-37-5,Silane, [[(6R)-6-(1,1-dimethylethyl)-1-cyclohexen-1-yl]oxy]trimethyl-

127082-37-5

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Basic information

Product Name: Silane, [[(6R)-6-(1,1-dimethylethyl)-1-cyclohexen-1-yl]oxy]trimethyl-
Synonyms:
CAS NO:127082-37-5
Molecular Formula: C13H26OSi
Molecular Weight: 226.434
EINECS: N/A
Product Categories: N/A
Mol File: 127082-37-5.mol
Article Data: 1

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: Silane, [[(6R)-6-(1,1-dimethylethyl)-1-cyclohexen-1-yl]oxy]trimethyl-(CAS DataBase Reference)
NIST Chemistry Reference: Silane, [[(6R)-6-(1,1-dimethylethyl)-1-cyclohexen-1-yl]oxy]trimethyl-(127082-37-5)
EPA Substance Registry System: Silane, [[(6R)-6-(1,1-dimethylethyl)-1-cyclohexen-1-yl]oxy]trimethyl-(127082-37-5)

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: 127082-37-5(Hazardous Substances Data)

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127082-37-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127082-37-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,8 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 127082-37:
(8*1)+(7*2)+(6*7)+(5*0)+(4*8)+(3*2)+(2*3)+(1*7)=115
115 % 10 = 5
So 127082-37-5 is a valid CAS Registry Number.

127082-37-5Upstream product

127082-37-5Downstream Products

127082-41-1 Acetic acid (R)-6-tert-butyl-cyclohex-1-enyl ester

127082-37-5Relevant articles and documents

Kinetic resolution of racemic 2-substituted cyclohexanones by enantioselective deprotonation

Kim,Kawasaki,Nakajima,Koga

, p. 6537 - 6540 (1989)

Incomplete deprotonation of racemic 2-substituted cyclohexanones (dl-4) by chiral lithium amides (2) in the presence of trimethylsilyl chloride was found to give the corresponding trimethylsilyl enol ethers (5) and the unreacted ketones (4) in reasonably high enantiomeric excesses.

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