91362-51-5 Usage
Chemical structure
A derivative of benzenediamine and benzimidazole
Common uses
a. Synthesis of pharmaceuticals and organic compounds
b. Acting as a ligand in coordination chemistry
c. Production of dyes, pigments, and polymers
d. Potential applications in medicinal chemistry
Reactivity
Forms stable complexes with metal ions
Safety concerns
May be hazardous to human health and the environment
Handling precautions
Handle with caution and follow safety guidelines
Unique structure
Contains both benzene and benzimidazole moieties
Potential applications
a. Development of new drugs and pharmaceuticals
b. Enhancement of existing drug properties
c. Research in coordination chemistry and metal ion interactions
d. Development of new dyes, pigments, and polymers with improved properties
Environmental impact
Potentially harmful to the environment if not handled properly
Regulatory considerations
May be subject to specific handling, storage, and disposal regulations depending on the jurisdiction.
Check Digit Verification of cas no
The CAS Registry Mumber 91362-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,6 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 91362-51:
(7*9)+(6*1)+(5*3)+(4*6)+(3*2)+(2*5)+(1*1)=125
125 % 10 = 5
So 91362-51-5 is a valid CAS Registry Number.
91362-51-5Relevant articles and documents
Electrochemical reduction of quinoxalinoquinoxaline: a revised mechanism
Armand, Joseph,Boulares, Line,Bellec, Christian,Bois, Claudette,Philoche-Levisalles, Michele,Pinson, Jean
, p. 1028 - 1030 (2007/10/02)
The electrochemical reduction of fluoflavine 2 gives compound 9 to which we had previously assigned a hexahydro-quinoxalinoquinoxaline structure.A crystallographic study of a diacetylated derivative of 9 shows that 9 is in fact 2-(o-aminoanilinomethyl)benzimidazole.This result permits us to propose a detailed reduction mechanism for 2 and its diacetyl derivative 25.
