78502-81-5 Usage
Description
5-BROMO-2-METHYL-4-PHENYL-1,3-THIAZOLE is a chemical compound with the molecular formula C10H8BrNS. It is a thiazole derivative containing a bromine atom, a methyl group, and a phenyl group. 5-BROMO-2-METHYL-4-PHENYL-1,3-THIAZOLE is known for its potential biological activities and diverse pharmacological properties, including antimicrobial, antiviral, anti-inflammatory, and anticancer activities. The presence of the bromine atom in this compound also makes it suitable for further functionalization and modification to create new drug candidates and chemical products.
Uses
Used in Organic Synthesis:
5-BROMO-2-METHYL-4-PHENYL-1,3-THIAZOLE is used as a building block in organic synthesis for the preparation of various thiazole-based compounds. Its unique structure allows for the creation of new chemical products with potential applications in various industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-BROMO-2-METHYL-4-PHENYL-1,3-THIAZOLE is used as a starting material for the development of new drug candidates. Its diverse pharmacological properties make it a promising candidate for the treatment of various diseases and conditions, including infections, inflammation, and cancer.
Used in Antimicrobial Applications:
5-BROMO-2-METHYL-4-PHENYL-1,3-THIAZOLE is used as an antimicrobial agent, exhibiting activity against a range of microorganisms. Its ability to inhibit the growth of bacteria, viruses, and other pathogens makes it a valuable component in the development of new antimicrobial drugs and treatments.
Used in Antiviral Applications:
In antiviral research, 5-BROMO-2-METHYL-4-PHENYL-1,3-THIAZOLE is used to develop compounds that can inhibit viral replication and reduce the severity of viral infections. Its antiviral properties make it a potential candidate for the treatment of various viral diseases.
Used in Anti-inflammatory Applications:
5-BROMO-2-METHYL-4-PHENYL-1,3-THIAZOLE is used as an anti-inflammatory agent, helping to reduce inflammation and alleviate symptoms associated with inflammatory conditions. Its potential to modulate inflammatory pathways makes it a promising candidate for the development of new anti-inflammatory drugs.
Used in Anticancer Applications:
In cancer research, 5-BROMO-2-METHYL-4-PHENYL-1,3-THIAZOLE is used to develop compounds with anticancer properties. Its ability to inhibit tumor growth and progression makes it a valuable component in the development of new cancer therapies and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 78502-81-5 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, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 78502-81:
(7*7)+(6*8)+(5*5)+(4*0)+(3*2)+(2*8)+(1*1)=145
145 % 10 = 5
So 78502-81-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H8BrNS/c1-7-12-9(10(11)13-7)8-5-3-2-4-6-8/h2-6H,1H3
78502-81-5Relevant articles and documents
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.
