14731-27-2 Usage
General Description
5-Benzylamino-[1,3,4]thiadiazole-2-thiol is a chemical compound with a complex structure that contains a benzylamino group and a thiadiazole-2-thiol group. It is commonly used in organic synthesis and medicinal chemistry as it exhibits a wide range of pharmacological activities. 5-BENZYLAMINO-[1,3,4]THIADIAZOLE-2-THIOL has been studied for its potential application in the treatment of various diseases, including cancer, diabetes, and cardiovascular disorders. Its unique structure and properties make it a valuable target for further research and development in the field of drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 14731-27-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,3 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14731-27:
(7*1)+(6*4)+(5*7)+(4*3)+(3*1)+(2*2)+(1*7)=92
92 % 10 = 2
So 14731-27-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9N3S2/c13-9-12-11-8(14-9)10-6-7-4-2-1-3-5-7/h1-5H,6H2,(H,10,11)(H,12,13)
14731-27-2Relevant articles and documents
Synthesis and optimization of thiadiazole derivatives as a novel class of substrate competitive c-Jun N-terminal kinase inhibitors
De, Surya K.,Chen, Vida,Stebbins, John L.,Chen, Li-Hsing,Cellitti, Jason F.,Machleidt, Thomas,Barile, Elisa,Riel-Mehan, Megan,Dahl, Russell,Yang, Li,Emdadi, Aras,Murphy, Ria,Pellecchia, Maurizio
scheme or table, p. 590 - 596 (2010/05/02)
A series of thiadiazole derivatives has been designed as potential allosteric, substrate competitive inhibitors of the protein kinase JNK. We report on the synthesis, characterization and evaluation of a series of compounds that resulted in the identifica
Synthesis and fungitoxicity of some 5-arylamino-2-polynitroarylthio-1,3,4-thiadiazoles
Sangal,Kumar
, p. 811 - 812 (2007/10/02)
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