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53744-76-6

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53744-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53744-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,4 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53744-76:
(7*5)+(6*3)+(5*7)+(4*4)+(3*4)+(2*7)+(1*6)=136
136 % 10 = 6
So 53744-76-6 is a valid CAS Registry Number.

53744-76-6SDS

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 2-cyano-N-phenylethanethioamide

1.2 Other means of identification

Product number -
Other names Ethanethioamide,2-cyano-N-phenyl

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:53744-76-6 SDS

53744-76-6Relevant articles and documents

COPOLYMER, PHOTOSENSITIVE RESIN COMPOSITION COMPRISING THE SAME AND COLOR FILTER

-

, (2020/05/20)

The present invention relates to a copolymerization polymer which is derived from a compound represented by chemical formula 1 and is usable as a dye, a photosensitive resin composition comprising the copolymerization polymer as a colorant, and to a color filter manufactured by using the photosensitive resin composition. In the chemical formula 1, each substituent group is the same as defined in the specification.

PROCESS FOR PREPARING 3-AMINOTHIENOPYRIDONE DERIVATIVES

-

Page 28, (2008/06/13)

This invention provides a class of 3-amino-7H-thieno[2,3-b]pyridin-6-one derivatives, substituted in the 7-position by an aryl, heteroaryl, cycloalkyl or heterocycloalkyl moiety, and in the 2-position by a specified range of substituent groups; also provided is a process for preparing those compounds, and the use thereof as intermediates in the manufacture of certain p38 MAP kinase inhibitors.

SYNTHESIS AND PROPERTIES OF 5-AMINO-1,2,3-THIADIAZOLE-4-CARBOTHIOAMIDES

Dankova, E. F.,Bakulev, V. A.,Kolobov, M. Yu.,Shishkina, V. I.,Yasman, Ya. B.,Lebedev, A. T.

, p. 1051 - 1055 (2007/10/02)

5-Amino-1,2,3-thiadiazole-4NR-carboxamides were reacted with P4S10, and 5-NR-amino-1,2,3-thiadiazole-4-carbonitriles with H2S.The reversible rearrangement of 5-amino-1,2,3-thiadiazole-4-NR-carbothioamides to 5-NR-amino-1,2,3-thiadiazole-4-carbothioamides

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