73040-66-1 Usage
Uses
Used in Pharmaceutical Industry:
2-Amino-5-(4-chlorophenyl)thiazole is used as an intermediate in the synthesis of pharmaceuticals for its antimicrobial and anticancer properties. It serves as a potential candidate for drug development, offering therapeutic benefits in treating infections and cancer.
Used in Agrochemical Industry:
2-Amino-5-(4-chlorophenyl)thiazole is used as a bioactive component in the development of agrochemicals, such as pesticides and herbicides. Its effectiveness against certain pests and weeds makes it a valuable asset in agricultural applications, contributing to crop protection and yield enhancement.
Used in Chemical Research:
2-Amino-5-(4-chlorophenyl)thiazole is utilized in chemical research for its unique structural and functional properties. It aids in the exploration of new chemical reactions, synthesis methods, and potential applications in various industries, further expanding its impact on science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 73040-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,4 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73040-66:
(7*7)+(6*3)+(5*0)+(4*4)+(3*0)+(2*6)+(1*6)=101
101 % 10 = 1
So 73040-66-1 is a valid CAS Registry Number.
73040-66-1Relevant academic research and scientific papers
Synthesis, characterization, and study the inhibitory effect of thiazole and thiadiazole derivatives toward the corrosion of copper in acidic media
Tomi, Ivan Hameed R.,Al-Daraji, Ali H. R.,Aziz, Sherien A.
, p. 605 - 613 (2015/02/02)
The authors describe the synthesis and characterization of two different five-member heterocycle derivatives (thiazole and thiadiazole) by several organic procedures. These compounds were characterized by FTIR, 1H NMR, and elemental analyses. A
Thiazolides as novel antiviral agents. 1. Inhibition of hepatitis B virus replication
Stachulski, Andrew V.,Pidathala, Chandrakala,Row, Eleanor C.,Sharma, Raman,Berry, Neil G.,Iqbal, Mazhar,Bentley, Joanne,Allman, Sarah A.,Edwards, Geoffrey,Helm, Alison,Hellier, Jennifer,Korba, Brent E.,Semple, J. Edward,Rossignol, Jean-Francois
scheme or table, p. 4119 - 4132 (2011/08/05)
We report the syntheses and activities of a wide range of thiazolides [viz., 2-hydroxyaroyl-N-(thiazol-2-yl)amides] against hepatitis B virus replication, with QSAR analysis of our results. The prototypical thiazolide, nitazoxanide [2-hydroxybenzoyl-N-(5-
