28771-82-6 Usage
Uses
Used in Pharmaceutical Industry:
5-BROMO-4-METHYL-2-PHENYL-1,3-THIAZOLE is used as a building block for the synthesis of biologically active molecules due to its unique structure and potential therapeutic properties.
Used in Organic Synthesis:
5-BROMO-4-METHYL-2-PHENYL-1,3-THIAZOLE is used as a reagent in organic synthesis, contributing to the creation of new compounds and materials.
Used in Chemical Research:
5-BROMO-4-METHYL-2-PHENYL-1,3-THIAZOLE is utilized in chemical research to explore its properties and potential applications, including its anti-cancer, anti-inflammatory, and antimicrobial capabilities.
Used in Drug Development:
5-BROMO-4-METHYL-2-PHENYL-1,3-THIAZOLE is employed in drug development as a precursor for the production of pharmaceuticals that target various diseases and conditions, leveraging its studied therapeutic effects.
Used in Antimicrobial Agents:
5-BROMO-4-METHYL-2-PHENYL-1,3-THIAZOLE is used as a component in the development of antimicrobial agents, given its potential to combat microbial infections.
Used in Anti-inflammatory Agents:
5-BROMO-4-METHYL-2-PHENYL-1,3-THIAZOLE is used in the formulation of anti-inflammatory agents, capitalizing on its potential to reduce inflammation.
Used in Anticancer Agents:
5-BROMO-4-METHYL-2-PHENYL-1,3-THIAZOLE is used in the development of anticancer agents, focusing on its potential to inhibit cancer cell growth and proliferation.
Check Digit Verification of cas no
The CAS Registry Mumber 28771-82-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,7,7 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28771-82:
(7*2)+(6*8)+(5*7)+(4*7)+(3*1)+(2*8)+(1*2)=146
146 % 10 = 6
So 28771-82-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H8BrNS/c1-7-9(11)13-10(12-7)8-5-3-2-4-6-8/h2-6H,1H3
28771-82-6Relevant articles and documents
IMIDAZOPYRIDAZINE COMPOUNDS
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Page/Page column 30, (2008/06/13)
The present invention relates to novel substituted imidazo[1,2-b]pyridazine compounds of Formula (I): pharmaceutical compositions thereof, and the use such compounds as corticotropin releasing factor 1 (CRF1) receptor antagonists in the treatment of psychiatric disorders and neurological diseases.
Thermally irreversible photochromic systems. Reversible photocyclization of 1,2-bis(thiazolyl)perfluorocyclopentenes
Uchida, Kingo,Ishikawa, Takayuki,Takeshita, Michinori,Irie, Masahiro
, p. 6627 - 6638 (2007/10/03)
Diarylethenes having thiazole rings, 1,2-bis(thiazol-4'- yl)perfluorocyclopentenes and 1,2-bis(thiazol-5'-yl)perfluorocyclopentences, were synthesized. The binding positions of the thiazole rings to the perfluorocyclopentene moiety strongly affected the a
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.
