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Trimethyl-[(E)-1-methyl-3-(2,6,6-trimethyl-cyclohex-1-enyl)-allyloxy]-silane is a complex organic compound with the molecular formula C14H27OSi. It is a colorless liquid at room temperature and is characterized by its unique structure, which includes a cyclohexene ring with three methyl groups, an allyl group, and a trimethylsilyl group. Trimethyl-[(E)-1-methyl-3-(2,6,6-trimethyl-cyclohex-1-enyl)-allyloxy]-silane is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds through the allylation reaction. It is also known for its stability and ability to participate in various chemical transformations, making it a valuable tool in the field of organic chemistry.

35156-37-7

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35156-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35156-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,5 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35156-37:
(7*3)+(6*5)+(5*1)+(4*5)+(3*6)+(2*3)+(1*7)=107
107 % 10 = 7
So 35156-37-7 is a valid CAS Registry Number.

35156-37-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-trimethyl((4-(2,6,6-trimethylcyclohex-1-en-1-yl)but-3-en-2-yl)oxy)silane

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:35156-37-7 SDS

35156-37-7Relevant academic research and scientific papers

NICKEL BORIDE REDUCTIVE CLEAVAGE OF ALLYLIC TRIMETHYLSILYL ETHERS

Sarma, D. N.,Sharma, R. P.

, p. 371 - 372 (1985)

Nickel boride reductive cleavage of allylic trimethylsilyl ethers yielding alkenes is described.

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