80379-64-2 Usage
Uses
Used in Pharmaceutical Industry:
(6E)-6-(morpholin-4-ylmethylidene)-2-phenyl-5,6-dihydro-1,3-benzothiazol-7(4H)-one is used as a pharmaceutical candidate for its potential anti-inflammatory and anti-tumor properties. (6E)-6-(morpholin-4-ylmethylidene)-2-phenyl-5,6-dihydro-1,3-benzothiazol-7(4H)-one's ability to modulate various biological pathways involved in inflammation and tumor growth makes it a valuable asset in the development of new therapeutic agents.
Used in Drug Design and Development:
In the field of drug design and development, (6E)-6-(morpholin-4-ylmethylidene)-2-phenyl-5,6-dihydro-1,3-benzothiazol-7(4H)-one serves as a key compound for exploring novel therapeutic strategies. Its unique chemical structure and potential biological activities provide a foundation for the creation of new drugs that could target a range of diseases, particularly those related to inflammation and cancer.
Used in Medicinal Chemistry Research:
(6E)-6-(morpholin-4-ylmethylidene)-2-phenyl-5,6-dihydro-1,3-benzothiazol-7(4H)-one is utilized as a subject of interest in medicinal chemistry research. (6E)-6-(morpholin-4-ylmethylidene)-2-phenyl-5,6-dihydro-1,3-benzothiazol-7(4H)-one's specific properties and potential applications make it a valuable tool for understanding the underlying mechanisms of various diseases and for identifying new targets for therapeutic intervention.
Check Digit Verification of cas no
The CAS Registry Mumber 80379-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,7 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80379-64:
(7*8)+(6*0)+(5*3)+(4*7)+(3*9)+(2*6)+(1*4)=142
142 % 10 = 2
So 80379-64-2 is a valid CAS Registry Number.
80379-64-2Relevant academic research and scientific papers
Condensation Reaction of 3,4-Dibenzoyl-1-methyl-2,5-diphenylpyrrole and -1-phenylpyrazole with Methylamine Derivatives Affording Pyrrolopyridine and 2H-Pyrazolo and pyridines
Mataka, Shuntaro,Takahashi, Kazufumi,Tashiro, Masashi
, p. 1073 - 1075 (2007/10/02)
The reaction of 3,4-dibenzoyl-1-methyl-2,5-diphenylpyrrole (1) and -1-phenylpyrazole (2) with methylamines (3a-c) afforded pyrrolopyridine (4), and isomeric 2H-pyrazolopyridines (5a-c) and pyridines (6a-c), respectively.
Reaction of Sulfene with Heterocyclic N,N-disubstituted α-Aminomethylketones. VII. Synthesis of 1,2-Oxathiinobenzothiazole Derivatives
Mosti, Luisa,Menozzi, Giulia,Schenone, Pietro
, p. 1069 - 1071 (2007/10/02)
The polar 1,4-cycloaddition of sulfene to N,N-disubstituted 6-aminomethylene-5,6-dihydro-2-phenylbenzothiazol-7-(4H)ones gave, generally in good yield, N,N-disubstituted 3,4,5,6-tetrahydro-8-phenyl-1,2-oxathiinobenzothiazol-4-amine 2,2-dioxides, which are derivatives af the new heterocyclic system 1,2-oxathiinobenzothiazole.This reaction did not occur only with the N,N-diphenylaminone.
