6963-77-5 Usage
Structure
A chemical compound containing a benzoimidazole ring with a sulfanylpropanoic acid group attached and a chloro substitution on the benzoimidazole ring.
Derivative of benzoimidazole
A chemical compound derived from the benzoimidazole structure.
Sulfanylpropanoic acid group
A functional group consisting of a sulfur atom bonded to a propanoic acid chain.
Use in pharmaceutical industry
Used as a potential inhibitor of certain enzymes and has been studied for its potential therapeutic effects in treating various diseases.
Building block in synthesis
Used as a starting material in the synthesis of other organic compounds.
Chloro substitution
The presence of a chlorine atom on the benzoimidazole ring, which makes the compound of interest for further research and development in the fields of medicine and organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 6963-77-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6963-77:
(6*6)+(5*9)+(4*6)+(3*3)+(2*7)+(1*7)=135
135 % 10 = 5
So 6963-77-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClN2O2S/c1-5(9(14)15)16-10-12-7-3-2-6(11)4-8(7)13-10/h2-5H,1H3,(H,12,13)(H,14,15)
6963-77-5Relevant articles and documents
Studies on synthesis of unsymmetrical 2,2′-bisbenzimidazole sulphides of pharmacological interest
Dubey,Naidu,Reddy, P.V.V. Prasada,Mahesh Kumar,Vineel, B. George
experimental part, p. 1443 - 1446 (2009/04/06)
Condensation of 2-(α-chloroethyl)benzimidazole 1 with benzimidazole-2-thiol 2 gives 2-(α-thioethyl-2′-benzimidazolyl)- benzimidazole 3. The latter can also be prepared by the reaction of 2-(α-thioethyl)benzimidazoie 4 with 2-chlorobenzimidazole 5. Alternatively, 3 can also be synthesized by the independent condensation of o-phenylenediamine 7 respectively with 2-(s-α-ethyl-o-ethyldithio- carbonate)benzimidazole 6 and with 2-(α-thiopropionic acid) benzimidazole 8. The structures of all the compounds synthesized have been established on the basis of their spectroscopic data.
