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2-Butenoic acid, 3-methyl-2-(phenylthio)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66716-63-0

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66716-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66716-63-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,7,1 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66716-63:
(7*6)+(6*6)+(5*7)+(4*1)+(3*6)+(2*6)+(1*3)=150
150 % 10 = 0
So 66716-63-0 is a valid CAS Registry Number.

66716-63-0SDS

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 methyl 3-methyl-2-phenylsulfanylbut-2-enoate

1.2 Other means of identification

Product number -
Other names methyl 3-methyl-2-phenylthiobut-2-enoate

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:66716-63-0 SDS

66716-63-0Relevant academic research and scientific papers

Synthesis of α-Phenylthio Enones and Esters of α-Phenylthio Alkenoic Acids

Durman, John,Grayson, J.Ian,Hunt, Paul G.,Warren, Stuart

, p. 1939 - 1946 (2007/10/02)

The title compounds can be made by a Pummerer dehydration from the corresponding saturated sulphoxides.The alkylation of anions from saturated and unsaturated ketones is described.

ALKYLATION OF EXTENDED ENOLATES FROM α-PHENYLTHIO CROTONATE ESTERS

Durman, John,Hunt, Paul G.,Warren, Stuart

, p. 2113 - 2116 (2007/10/02)

Conditions are described for the formation of enolate anions from substituted α-phenylthio-crotonate esters and their alkylation at the α-carbon atom.

Reactions of Benzenesulphenyl Chloride with α,β-Unsaturated Compounds: Part II - Role of Steric Factors on Stability of Intermediates

Bhongle, N. N.,Gogte, V. N.

, p. 632 - 636 (2007/10/02)

In presence of pyridine, benzenesulfphenyl chloride (1) adds on the methyl α- and β-methyl crotonates and methyl α- and β-methyl cinnamates (6-9) in regiospecific manner involving an onium intermediate such as (18).The product pattern is decided by the st

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