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Ethyl 5-bromo-4-methylthiazole-2-carboxylate is a chemical compound characterized by the molecular formula C8H8BrNO2S. It is a yellow solid that is soluble in various organic solvents and possesses a distinctive odor. Ethyl 5-bromo-4-methylthiazole-2-carboxylate is recognized for its potential reactivity and toxicity, necessitating careful handling and storage under controlled conditions.
Used in Pharmaceutical Industry:
Ethyl 5-bromo-4-methylthiazole-2-carboxylate is utilized as a building block for the synthesis of a variety of pharmaceutical compounds. Its role in the development and production of pharmaceuticals is vital, contributing to the creation of new medications and therapies.
Used in Organic Synthesis:
In the field of organic synthesis, Ethyl 5-bromo-4-methylthiazole-2-carboxylate serves as a reagent for the preparation of heterocyclic compounds. Its application in this area is instrumental in advancing the synthesis of complex organic molecules and expanding the scope of organic chemistry.

79247-80-6

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79247-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79247-80-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,4 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79247-80:
(7*7)+(6*9)+(5*2)+(4*4)+(3*7)+(2*8)+(1*0)=166
166 % 10 = 6
So 79247-80-6 is a valid CAS Registry Number.

79247-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-bromo-4-methyl-1,3-thiazole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 5-bromo-4-methyl-thiazole-2-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:79247-80-6 SDS

79247-80-6Downstream Products

79247-80-6Relevant academic research and scientific papers

Relationship between mechanochromic behavior and crystal structures in donor-π-acceptor compounds consisted of aromatic rings with ester moiety as an acceptor

Matsumoto, Shoji,Moteki, Jun,Ito, Yuji,Akazome, Motohiro

supporting information, p. 3512 - 3516 (2017/10/05)

We investigated the mechanochromic behavior of donor-π-acceptor compounds which consisted of diphenylaminophenylacetylene as a donor-π moiety and (hetero)aromatic ring bearing ester as an acceptor. The compounds with dicyanobenzoic ester gave the bathochr

HETEROCYCLIC DERIVATIVES FOR THE TREATMENT OF DISEASES

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Page/Page column 102, (2011/11/30)

The invention relates to compounds of Formula (1) and to processes for the preparation of, intermediates used in the preparation of, compositions containing and the uses of, such derivatives. The compounds according to the present invention are useful in numerous diseases in which ALK protein is involved or in which inhibition of ALK activity may induce benefit, especially for the treatment of cancer mediated by a mutated EML4-ALK fusion protein.

THIAZOLE AMIDES, IMIDAZOLE AMIDES AND RELATED ANALOGUES

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Page/Page column 46, (2008/06/13)

Thiazole amides, imidazole amides and related analogues of the Formula: are provided, in which variables are as described herein. Such compounds may be used to modulate ligand binding to histamine H3 receptors in vivo or in vitro, and are particularly use

An Infrared Study of Rotational Isomerism in Thiazole-2-carboxylates

Kaye, Perry T.,Meakins, G. Denis,Willbe, Charles,Williams, Peter R.

, p. 2335 - 2339 (2007/10/02)

A series of alkyl thiazole-2-carboxylates containing a range of substituents at the 4- and 5-positions has been prepared.Solutions of these esters (mostly new compounds) show well resolved doublets in the i.r.C=O region which arise from rotational isomers.The higher wavenumber components are assigned to the more polar carbonyl O,S-anti-s-trans-rotamers and the lower wavenumber components to the carbonyl O,S-syn-s-trans-forms.Small, but systematic, differences between the methyl esters are noted.

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