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Cyclohexanone, 2-[3-(phenylthio)-2-propenyl]-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102438-35-7

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102438-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102438-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,3 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 102438-35:
(8*1)+(7*0)+(6*2)+(5*4)+(4*3)+(3*8)+(2*3)+(1*5)=87
87 % 10 = 7
So 102438-35-7 is a valid CAS Registry Number.

102438-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-2-[3-(phenylthio)prop-2-en-1-yl]cyclohexanone

1.2 Other means of identification

Product number -
Other names (E)-2-(3-phenylthioallyl)cyclohexanone

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:102438-35-7 SDS

102438-35-7Relevant academic research and scientific papers

Readily prepared 3-Chloro-1 -(phenylthio)propene, a versatile three-carbon annulating agent

Liu, Taoping,Zhao, Xiaoming,Lu, Long,Cohen, Theodore

supporting information; experimental part, p. 4576 - 4579 (2009/12/07)

3-Chloro-1-(phenylthio)propene, simply generated by chlorination of commercial allyl phenyl sulfide, is a versatile 3-carbon annulating agent for ketones and phenols.

Allylation with substituted vinylthionium ions from SnCl4 ionisation of 1,3- and 3,3-bis(alkyl/phenylthio)propenes

Hunter,Michael,Walter

, p. 9377 - 9398 (2007/10/02)

α- and γ-substituted vinylthionium ions from SnCl4 ionisation of a range of substituted 1,3- and 3,3-bis(alkyl/phenylthio)propenes allylate enol silyl ethers in good yield. Levels of regioselectivity are sterically dependent and in the case of

Alkylation of enol silyl ethers with vinylthionium ions generated from 1,1- and 1,3-bis(phenylthio)propenes

Hunter, Roger,Michael, Joseph P.,Walter, Daryl S.

, p. 5413 - 5416 (2007/10/02)

Vinylthionium ions generated from 1,1- and 1,3-bis-(phenylthio) propenes alkylate enol silyl ethers regioselectively under mild reaction conditions with tin tetrachloride.

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