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2-CHLORO-4-PHENYL-5-THIAZOLECARBOXYLIC ACID ETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74476-47-4

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74476-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74476-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,7 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74476-47:
(7*7)+(6*4)+(5*4)+(4*7)+(3*6)+(2*4)+(1*7)=154
154 % 10 = 4
So 74476-47-4 is a valid CAS Registry Number.

74476-47-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-phenylthiazole-5-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 2-Chloro-4-phenyl-thiazole-5-carboxylic acid ethyl 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:74476-47-4 SDS

74476-47-4Relevant academic research and scientific papers

Thiazolyl-benzimidazoles

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Page/Page column 40, (2008/06/13)

The invention is directed to compounds of formula (1) [image] and pharmaceutically acceptable salts thereof, methods for the preparation thereof, and methods of use thereof.

THIAZOLE COMPOUNDS AND THEIR USE AS PGD2 ANTAGONISTS

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Page/Page column 35-36, (2008/06/13)

A compound for use as a PGD2 antagonist is of structural formula [1] in which: A represents a fully saturated or partially unsaturated monocyclic 5-7 membered ring containing one or two nitrogen atoms; B represents a direct bond, an optionally substituted

Syntheses and Reactions of 2-Halo-5-thiazolecarboxylates

Lee, Len F.,Schleppnik, Francis M.,Howe, Robert K.

, p. 1621 - 1630 (2007/10/02)

A variety of 2-halo-5-thiazolecarboxylates was prepared from substituted-3-aminoacrylates and 3-ketoesters.Selective reduction of 2-chloro-5-thiazolecarboxylates 4a, 4i and 4j with sodium borohydride in ethanol provided the corresponding 2-halo-5-thiazolemethanols 27 - 29.Nucleophilic displacement on methyl methanesulfonate (32c) occured selectivity at the 5-substituent to provide 2-chloro-4-(trifluoromethyl)-5-(heteroatom-substituted methyl)thiazoles 32d-f.

2-Substituted-4-aryl-5-thiazolecarboxylic acids and their derivatives as safening agents

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, (2008/06/13)

These compounds have been found to be effective in reducing herbicidal injury to direct-seeded rice caused by 2-chloro-2',6'-diethyl-N-(butoxymethyl)acetanilide.

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