35342-50-8 Usage
Uses
Used in Pharmaceutical Industry:
5-BROMO-2,4-DIPHENYL-1,3-THIAZOLE is used as a potential pharmaceutical agent for its anti-cancer, anti-viral, and anti-inflammatory properties. Its unique structure and functional groups contribute to its therapeutic potential in various medical applications.
Used in Organic Synthesis:
5-BROMO-2,4-DIPHENYL-1,3-THIAZOLE is used as a building block in the synthesis of other organic compounds. Its presence of bromine atom and phenyl groups allows for further chemical reactions and modifications, leading to the development of new compounds with desired properties.
Used in Research and Development:
5-BROMO-2,4-DIPHENYL-1,3-THIAZOLE is used as a research tool in the study of thiazole chemistry and pharmacology. Its unique structure and properties make it valuable for understanding the behavior of thiazole derivatives and their potential applications in drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 35342-50-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,4 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35342-50:
(7*3)+(6*5)+(5*3)+(4*4)+(3*2)+(2*5)+(1*0)=98
98 % 10 = 8
So 35342-50-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H10BrNS/c16-14-13(11-7-3-1-4-8-11)17-15(18-14)12-9-5-2-6-10-12/h1-10H
35342-50-8Relevant academic research and scientific papers
In-Depth Assessment of the Palladium-Catalyzed Fluorination of Five-Membered Heteroaryl Bromides
Milner, Phillip J.,Yang, Yang,Buchwald, Stephen L.
supporting information, p. 4775 - 4780 (2015/10/28)
A thorough investigation of the challenging Pd-catalyzed fluorination of five-membered heteroaryl bromides is presented. Crystallographic studies and density functional theory (DFT) calculations suggest that the challenging step of this transformation is
Palladium-catalyzed cross-coupling reaction of haloazoles with phenylsulfonylacetonitrile
Sakamoto,Kondo,Suginome,Ohba,Yamanaka
, p. 552 - 554 (2007/10/02)
Condensation of halo-substituted 1,3-azoles (1,3-oxazoles, 1,3-thiazoles and imidazoles) with phenylsulfonylacetonitrile under basic conditions was promoted by catalytic action of tetrakis(triphenylphosphine)palladium(0) to give α-phenylsulfonyl-1,3-azole
