Cas 127020-68-2,1-[(E)-3-(tert-Butyl-dimethyl-silanyloxy)-propenyl]-3-methyl-2-oxo-cyclohexanecarboxylic acid benzyl ester

127020-68-2

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Basic information

Product Name: 1-[(E)-3-(tert-Butyl-dimethyl-silanyloxy)-propenyl]-3-methyl-2-oxo-cyclohexanecarboxylic acid benzyl ester
Synonyms:
CAS NO:127020-68-2
Molecular Formula:
Molecular Weight: 416.633
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: 1-[(E)-3-(tert-Butyl-dimethyl-silanyloxy)-propenyl]-3-methyl-2-oxo-cyclohexanecarboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-[(E)-3-(tert-Butyl-dimethyl-silanyloxy)-propenyl]-3-methyl-2-oxo-cyclohexanecarboxylic acid benzyl ester(127020-68-2)
EPA Substance Registry System: 1-[(E)-3-(tert-Butyl-dimethyl-silanyloxy)-propenyl]-3-methyl-2-oxo-cyclohexanecarboxylic acid benzyl ester(127020-68-2)

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: 127020-68-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127020-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,2 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 127020-68:
(8*1)+(7*2)+(6*7)+(5*0)+(4*2)+(3*0)+(2*6)+(1*8)=92
92 % 10 = 2
So 127020-68-2 is a valid CAS Registry Number.

127020-68-2Upstream product

127020-68-2Downstream Products

127020-45-5 2-[(E)-3-(tert-Butyl-dimethyl-silanyloxy)-propenyl]-6-methyl-cyclohexanone

127020-68-2Relevant academic research and scientific papers

A controlled synthesis of α-(E)-1-alkenyl ketones from β-keto benzyl esters

Hashimoto,Miyazaki,Shinoda,Ikegami

, p. 7195 - 7198 (1989)

A regio- and stereocontrolled method for the synthesis of α-(E)-1-alkenyl ketones from β-keto benzyl esters has been developed by devising the sequence of a modified Pinhey's alkenylation and a reductive removal of a benzyloxycarbonyl group with Raney nic

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