175135-68-9 Usage
Uses
Used in Pharmaceutical Industry:
2-[(5-Amino-1,3,4-thiadiazol-2-yl)thio]-5-nitrobenzonitrile is used as an intermediate in the synthesis of pharmaceuticals for its potential biological and pharmacological applications. The presence of the amino and nitro groups allows for the development of compounds with specific therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical industry, 2-[(5-Amino-1,3,4-thiadiazol-2-yl)thio]-5-nitrobenzonitrile is utilized as an intermediate in the production of agrochemicals, potentially contributing to the development of new pesticides or other agricultural products due to its unique molecular structure and functional groups.
Used in Research and Development:
2-[(5-Amino-1,3,4-thiadiazol-2-yl)thio]-5-nitrobenzonitrile is used as a subject of research and development for its potential biological activities. The thiadiazole moiety and the presence of amino and nitro groups make it an interesting candidate for exploring new therapeutic agents or other applications in the fields of biology and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 175135-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,3 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 175135-68:
(8*1)+(7*7)+(6*5)+(5*1)+(4*3)+(3*5)+(2*6)+(1*8)=139
139 % 10 = 9
So 175135-68-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H5N5O2S2/c10-4-5-3-6(14(15)16)1-2-7(5)17-9-13-12-8(11)18-9/h1-3H,(H2,11,12)
175135-68-9Relevant academic research and scientific papers
Design and synthesis of new heterocyclic Bcr-Abl inhibitors
Chen, Yong-Fei,Ni, Nanting,Li, Minyong,Xu, Peng-Fei,Wang, Binghe
experimental part, p. 123 - 135 (2011/06/26)
Herein, a series of heterocyclic Bcr-Abl kinase inhibitors with different structural scaffolds were designed and synthesized. HTScan Abll kinase assay kit was used for the inhibitory test. Some modest inhibitors were obtained.