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389891-34-3

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389891-34-3 Usage

Common use

Photoinitiator for free radical polymerization reactions, particularly in production of printing inks and coatings

Physical appearance

Yellow to orange powder

Melting point

130-134°C

Solubility

Soluble in organic solvents like acetone and ethyl acetate

Potential applications

Adhesives, rubber, electronic materials

Check Digit Verification of cas no

The CAS Registry Mumber 389891-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,8,9 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 389891-34:
(8*3)+(7*8)+(6*9)+(5*8)+(4*9)+(3*1)+(2*3)+(1*4)=223
223 % 10 = 3
So 389891-34-3 is a valid CAS Registry Number.

389891-34-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(5-cyano-2-methoxyphenyl)thioacrylic acid S-benzothiazol-2-yl-thioester

1.2 Other means of identification

Product number -
Other names (E)-3-(5-cyano-2-methoxy-phenyl)-thioacrylic acid S-benzothiazol-2-yl ester

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:389891-34-3 SDS

389891-34-3Relevant articles and documents

Beating the hydrogen bond: First selective and high-yielding N-acylation process for an α,β-diaminoalcohol

Storz, Thomas,Dittmar, Peter,Grimler, Dominique,Testa, Maria,Potgeter, Heiko,Chappel, Didier,Hartmann, Otto,Niederer, Daniel,Trueby, Martin

, p. 1184 - 1191 (2012/12/23)

The first selective and high-yielding N-acylation of an α,β-diaminoalcohol is reported, as well as the first use as N-acylation agent of a 5-mercaptobenzothiazolyl thioester of an α,β-unsaturated carboxylic acid. Other conventional coupling methods (acid

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