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5-Thiazolecarboxylicacid,2-amino-4-ethyl-,ethylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72850-74-9

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72850-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72850-74-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,5 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72850-74:
(7*7)+(6*2)+(5*8)+(4*5)+(3*0)+(2*7)+(1*4)=139
139 % 10 = 9
So 72850-74-9 is a valid CAS Registry Number.

72850-74-9SDS

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 ethyl 2-amino-4 ethylthiazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl-2-amino-4-ethyl-5-thiazolcarboxylat

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:72850-74-9 SDS

72850-74-9Downstream Products

72850-74-9Relevant academic research and scientific papers

BI-ARYL DIHYDROOROTATE DEHYDROGENASE INHIBITORS

-

Page/Page column 200; 223, (2021/04/17)

Disclosed are compounds, compositions and methods for treating diseases, disorders, or medical conditions that are affected by the modulation of DHODH. Such compounds are represented by Formula I as follows: Formula I wherein R1, R2, R3, and Q are defined herein.

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-Amino-4-substituted-thiazolecarboxylic acids and their derivatives

-

, (2008/06/13)

2-Amino-4-substituted-5-thiazolecarboxylic acids and derivatives thereof, are intermediates for the preparation of 2-substituted-4-substituted-5-thiazolecarboxylic acid derivatives which are herbicidal safeners.

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