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Benzenecarbodithioic acid, 2-propenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27249-64-5

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27249-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27249-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,4 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27249-64:
(7*2)+(6*7)+(5*2)+(4*4)+(3*9)+(2*6)+(1*4)=125
125 % 10 = 5
So 27249-64-5 is a valid CAS Registry Number.

27249-64-5SDS

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 prop-2-enyl benzenecarbodithioate

1.2 Other means of identification

Product number -
Other names allyl dithiobenzoate

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:27249-64-5 SDS

27249-64-5Relevant academic research and scientific papers

Intramolecular Cyclization of (Allylthio)sulfines via their Vinylsulfenic Acid Tautomers

Mazzanti, Germana,Ruinaard, Rene,Vliet, Leonard A. van,Zani, Paolo,Bonini, Bianca F.,Zwanenburg, Binne

, p. 6383 - 6386 (1992)

Intramolecular cyclization of enethiolizable (allylthio)sulfines afford 2-alkylidene-1,3-dithiolane-1-oxides in good yields.The formation of these compounds can be explained by an initial tautomerization of the sulfine to vinyl sulfenic acid, followed by

-CYCLOADDITION OF DITHIOBENZOIC ESTERS TO DIPHENYLKETENE

Drozd, V. N.,Popova, O. A.

, p. 946 - 949 (2007/10/02)

Dithiobenzoic esters and diphenylketene react by a mechanism of -cycloaddition with the formation of 4-alkylthio-2-thietanones.During thermolysis and electron impact the products readilly undergo both the retro reaction with the formation of the initial structures and cyclodecomposition with the elimination of carbon sulfoxide.

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