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

78502-77-9

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78502-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78502-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,0 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78502-77:
(7*7)+(6*8)+(5*5)+(4*0)+(3*2)+(2*7)+(1*7)=149
149 % 10 = 9
So 78502-77-9 is a valid CAS Registry Number.

78502-77-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Thiazolecarboxylicacid,4-(bromomethyl)-,ethylester(9CI)

1.2 Other means of identification

Product number -
Other names 4-Brommethyl-5-thiazolcarbonsaeure-ethylester

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:78502-77-9 SDS

78502-77-9Relevant academic research and scientific papers

POSITIVE ALLOSTERIC MODULATORS OF THE MUSCARINIC ACETYLCHOLINE RECEPTOR M1

-

Paragraph 0293; 0294, (2019/11/11)

Described are positive allosteric modulators of muscarinic acetylcholine receptor M1 (mAChR M1), pharmaceutical compositions including the compounds, and methods of using the compounds and compositions for treating neurological disorders, psychiatric disorders, or a combination thereof.

N-Bromosuccinimide Bromination of Substituted Methylthiazoles

Krieg, Benno,Mittner, Juergen

, p. 623 - 632 (2007/10/02)

Bromination of methylthiazoles with one unsubstituted position by N-bromosuccinimide may take place either at the methyl group, at the heterocyclic nucleus, or at both positions according to the nature of the second substituent.The ethoxycarbonyl group in the compounds 1a-3a directs the bromine into the side chain.So it is possible to obtain the tribromomethyl compounds 1d and 2d without bromination of the thiazole nucleus.In the phenyl-substituted methylthiazoles 4a-6a bromination takes place in the methyl group and in the heterocyclic nucleus. - The bromomethylthiazoles 1b-3b yield the vinylthiazoles 1k-3k by Wittig reaction.

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