21160-50-9 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-BROMO-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals for its potential role in the development of new drugs. Its unique structural features and reactivity contribute to the creation of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(4-BROMO-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID serves as a building block for the synthesis of agrochemicals, including pesticides and herbicides, due to its ability to be incorporated into complex molecular structures with desired biological activities.
Used in Chemical Research and Drug Discovery:
2-(4-BROMO-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID is utilized as a research compound in chemical research and drug discovery processes. Its structural properties and reactivity make it a promising candidate for exploring new chemical reactions and developing innovative materials and drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 21160-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,1,6 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21160-50:
(7*2)+(6*1)+(5*1)+(4*6)+(3*0)+(2*5)+(1*0)=59
59 % 10 = 9
So 21160-50-9 is a valid CAS Registry Number.
21160-50-9Relevant academic research and scientific papers
THIAZOLEUREAS AS ANTICANCER AGENTS
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Page/Page column 114, (2020/03/02)
The invention relates to heterocyclic urea derivatives and their use in the treatment and prophylaxis of cancer, and to compositions containing said derivatives and processes for their preparation.
Synthesis and Biological Investigation of Oxazole Hydroxamates as Highly Selective Histone Deacetylase 6 (HDAC6) Inhibitors
Senger, Johanna,Melesina, Jelena,Marek, Martin,Romier, Christophe,Oehme, Ina,Witt, Olaf,Sippl, Wolfgang,Jung, Manfred
, p. 1545 - 1555 (2016/03/08)
Histone deacetylase 6 (HDAC6) catalyzes the removal of an acetyl group from lysine residues of several non-histone proteins. Here we report the preparation of thiazole-, oxazole-, and oxadiazole-containing biarylhydroxamic acids by a short synthetic proce
