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332099-36-2

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332099-36-2 Usage

General Description

3-Bromo-4(H)-thieno[3,2-b]pyrrole-5-carboxylic acid is a chemical compound that falls under the category of organic compounds known as pyrroles and thiophenes. Pyrroles are aromatic compounds containing a five-membered unsaturated ring of four carbon atoms and one nitrogen atom while, thiophenes are compounds containing a thiophene ring, which is a five-membered aromatic ring made up of four carbon atoms and one sulfur atom. The precise properties of 3-Bromo-4(H)-thieno[3,2-b]pyrrole-5-carboxylic acid, such as its molecular weight, boiling and melting points, and solubility, are dependent on its specific molecular structure. 3-BROMO-4(H)-THIENO[3,2-B]PYRROLE-5-CARBOXYLICACID can be used in chemical research and might be an intermediate in the synthesis of more complex chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 332099-36-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,0,9 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 332099-36:
(8*3)+(7*3)+(6*2)+(5*0)+(4*9)+(3*9)+(2*3)+(1*6)=132
132 % 10 = 2
So 332099-36-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrNO2S/c8-3-2-12-5-1-4(7(10)11)9-6(3)5/h1-2,9H,(H,10,11)

332099-36-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-4H-thieno[3,2-b]pyrrole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-bromo-4H-thieno[3,2-b]pyrrole-5-carboxylic acid

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:332099-36-2 SDS

332099-36-2Relevant articles and documents

Synthesis and CHK1 inhibitory potency of Hymenialdisine analogues

Parmentier, Jean-Gilles,Portevin, Bernard,Golsteyn, Roy M.,Pierré, Alain,Hickman, John,Gloanec, Philippe,De Nanteuil, Guillaume

scheme or table, p. 841 - 844 (2009/08/07)

A series of thieno[3,2-b]pyrroloazepinones derivatives related to Hymenialdisine were prepared and tested for CHK1 inhibitory activity. Nanomolar inhibitions were achieved when electron-withdrawing substituents were introduced at position 3 of the thiophene ring.

USE OF FUSED PYRROLE CARBOXYLIC ACIDS FOR THE TREATMENT OF NEURODEGENERATIVE AND PSYCHIATRIC DISEASES AS D-AMINO ACID OXIDASE INHIBITORS

-

Page/Page column 18, (2008/06/13)

The present invention provides the use of fused pyrrole carboxylic acids of formula (I) for the manufacture of a medicament to inhibit D-amino acid oxidase, particularly for the treatment of neurodegenerative and psychiatric disorders or diseases; certain

Bicyclic pyrrolyl amides as glycogen phosphorylase inhibitors

-

, (2008/06/13)

This invention relates to compounds of Formula I or stereoisomers, pharmaceutically acceptable salts or prodrugs thereof or a pharmaceutically acceptable salts of the prodrugs. This invention also relates to pharmaceutical compositions comprising a compou

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