914347-21-0 Usage
Uses
Used in Pharmaceutical Industry:
5-BROMO-2-PHENYLTHIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is used as a building block for the synthesis of pharmaceuticals due to its unique chemical structure and functional groups, which can be further modified to create new drug candidates.
Used in Agrochemical Industry:
In the agrochemical sector, 5-BROMO-2-PHENYLTHIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is utilized as a starting material for the development of new agrochemicals, potentially enhancing crop protection and yield through its antibacterial and antifungal properties.
Used in Organic Synthesis:
5-BROMO-2-PHENYLTHIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is employed as a versatile intermediate in organic synthesis, allowing for the creation of a variety of chemical compounds with different applications across various industries.
Used in Drug Discovery:
5-BROMO-2-PHENYLTHIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is used in drug discovery processes for its potential to contribute to the development of new drugs, particularly in the context of its demonstrated antibacterial and antifungal activities, which are crucial for addressing current and emerging health challenges.
Check Digit Verification of cas no
The CAS Registry Mumber 914347-21-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,3,4 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 914347-21:
(8*9)+(7*1)+(6*4)+(5*3)+(4*4)+(3*7)+(2*2)+(1*1)=160
160 % 10 = 0
So 914347-21-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H10BrNO2S/c1-2-16-12(15)9-10(13)17-11(14-9)8-6-4-3-5-7-8/h3-7H,2H2,1H3
914347-21-0Relevant articles and documents
I2/TBHP-Mediated tandem cyclization and oxidation reaction: Facile access to 2-substituted thiazoles and benzothiazoles
Liu, Li,Tan, Chen,Fan, Rong,Wang, Zihan,Du, Hongguang,Xu, Kun,Tan, Jiajing
, p. 252 - 256 (2019/01/10)
The efficient synthesis of 2-substituted thiazoles and benzothiazoles has been accomplished employing readily available cysteine esters and 2-aminobenzenethiols as N and S sources. The reaction proceeds under an I2/TBHP system and involves a on