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2-Pentenoic acid, 5-phenyl-2-(phenylsulfinyl)-, methyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138770-95-3

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138770-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138770-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,7 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138770-95:
(8*1)+(7*3)+(6*8)+(5*7)+(4*7)+(3*0)+(2*9)+(1*5)=163
163 % 10 = 3
So 138770-95-3 is a valid CAS Registry Number.

138770-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(benzenesulfinyl)-5-phenylpent-2-enoate

1.2 Other means of identification

Product number -
Other names methyl (E)-5-phenyl-2-(phenylsulphinyl)pent-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:138770-95-3 SDS

138770-95-3Relevant academic research and scientific papers

On the Preparation and Rearrangement of Some Vinylic Sulphoxides

Cass, Quezia B.,Jaxa-Chamiec, Albert A.,Kunec, Ellen K.,Sammes, Peter G.

, p. 2683 - 2686 (2007/10/02)

The condensation of methyl benzenesulphinylacetate 1 with a series of aldehydes has been explored using different catalysts.With zinc chloride, the enolate of 1 produces the conjugated ester directly.A base-catalysed rearrangement of these conjugated este

Preparation and Rearrangement of Some Conjugated Phenylsulphinylacetate Derivatives

Cass, Quezia B.,Jaxa-Chamiec, Albert A.,Sammes, Peter G.

, p. 1248 - 1250 (2007/10/02)

The direct condensation of saturated or unsaturated aldehydes with methyl phenylsulphinylacetate can be effected with the products undergoing base-catalysed rearrangements, those from saturated aldehydes yielding γ-hydroxy-αβ-unsaturated esters, whilst crotonaldehyde gives rise to methyl 6-phenylsulphinylhexa-2,4-dienoate.

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