321943-75-3 Usage
Description
4-Chloro-N-(6-nitrobenzo[d]thiazol-2-yl)benzaMide is a chemical compound with the molecular formula C14H8ClN3O4S. It is a benzamide derivative featuring a 4-chloro substitution and a nitrobenzothiazole moiety. 4-Chloro-N-(6-nitrobenzo[d]thiazol-2-yl)benzaMide possesses a unique structure and potential pharmacological properties, making it a promising candidate for pharmaceutical and research applications.
Uses
Used in Pharmaceutical Industry:
4-Chloro-N-(6-nitrobenzo[d]thiazol-2-yl)benzaMide is used as a building block for the synthesis of various organic compounds, contributing to the development of new drug candidates. Its unique structure and potential pharmacological properties make it a valuable component in the creation of innovative therapeutic agents.
Used in Research Applications:
In the field of research, 4-Chloro-N-(6-nitrobenzo[d]thiazol-2-yl)benzaMide serves as a starting material for the preparation of new compounds with potential applications in various scientific domains. Its properties and potential uses make it a valuable tool for further study and development, paving the way for advancements in multiple disciplines.
Check Digit Verification of cas no
The CAS Registry Mumber 321943-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,9,4 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 321943-75:
(8*3)+(7*2)+(6*1)+(5*9)+(4*4)+(3*3)+(2*7)+(1*5)=133
133 % 10 = 3
So 321943-75-3 is a valid CAS Registry Number.
321943-75-3Relevant articles and documents
Facile synthesis of N-acyl 2-aminobenzothiazoles by NHC-catalyzed direct oxidative amidation of aldehydes
Premaletha, Sethulekshmy,Ghosh, Arghya,Joseph, Sumi,Yetra, Santhivardhana Reddy,Biju, Akkattu T.
supporting information, p. 1478 - 1481 (2017/02/05)
A mild, general, and high yielding synthesis of N-acyl 2-aminobenzothiazoles has been demonstrated by N-heterocyclic carbene (NHC)-organocatalyzed direct amidation of aldehydes with 2-aminobenzothiazoles proceeding via acyl azolium intermediates. The carbene generated from the triazolium salt under oxidative conditions was the key for the success of this reaction. The method was subsequently applied to the synthesis of various biologically important N-acyl 2-aminobenzothiazoles.
