7612-96-6 Usage
Uses
Used in Organic Synthesis:
4-Phenylazophenyl isothiocyanate is used as a reagent in the synthesis of organic compounds, particularly for the formation of thioureas and carbamates through its reactions with amines and alcohols, respectively.
Used in Fluorescent Dyes and Pigments:
4-PHENYLAZOPHENYL ISOTHIOCYANATE is utilized as a reagent in the preparation of fluorescent dyes and pigments, contributing to its applications in various industries that require such materials for coloration and detection purposes.
Used in Medicinal Chemistry:
4-Phenylazophenyl isothiocyanate is used as a research compound in medicinal chemistry, where it is studied for its potential anti-tumor and anti-microbial properties, indicating its possible use in the development of new pharmaceuticals.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 4-Phenylazophenyl isothiocyanate is used as a key intermediate in the development of drugs that target specific biological pathways, potentially leading to the creation of novel therapeutic agents for various diseases, including cancer and microbial infections.
Check Digit Verification of cas no
The CAS Registry Mumber 7612-96-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,1 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7612-96:
(6*7)+(5*6)+(4*1)+(3*2)+(2*9)+(1*6)=106
106 % 10 = 6
So 7612-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H9N3S/c17-10-14-11-6-8-13(9-7-11)16-15-12-4-2-1-3-5-12/h1-9H/b16-15+
7612-96-6Relevant academic research and scientific papers
Identification of novel, selective and potent Chk2 inhibitors
Larson, Gary,Yan, Shunqi,Chen, Huanming,Rong, Frank,Hong, Zhi,Wu, Jim Zhen
, p. 172 - 175 (2007/10/03)
A series of isothiazole carboxamidine compounds were synthesized and discovered as novel and selective inhibitors for Chk2. They are not active against the related Chk1 kinase. The structure-activity relationship studies were performed on the scaffold, an
Synthesis of thiophene-2-carboxamidines containing 2-aminothiazoles and their biological evaluation as urokinase inhibitors
Wilson, Kenneth J.,Illig, Carl R.,Subasinghe, Nalin,Hoffman, James B.,Jonathan Rudolph,Soll, Richard,Molloy, Christopher J.,Bone, Roger,Green, David,Randall, Troy,Zhang, Marie,Lewandowski, Frank A.,Zhou, Zhao,Sharp, Celia,Maguire, Diane,Grasberger, Bruce,DesJarlais, Renee L.,Spurlino, John
, p. 915 - 918 (2007/10/03)
The serine protease urokinase (uPa) has been implicated in the progression of both breast and prostate cancer. Utilizing structure based design, the synthesis of a series of substituted 4-[2-amino-1,3-thiazolyl]-thiophene-2-carboxamidines is described. Further optimization of this series by substitution of the terminal amine yielded urokinase inhibitors with excellent activities.
