4615-69-4 Usage
Derivative of benzimidazole
A heterocyclic aromatic organic compound
Presence of nitro and oxide groups
Makes it potentially useful as a pharmaceutical intermediate
Potential use
In the synthesis of new drugs or as a starting material for the production of other organic compounds
Specific properties and uses
Depend on the specific applications and research or industrial processes involved
Chemical structure
Of particular interest for pharmaceutical and chemical research
Check Digit Verification of cas no
The CAS Registry Mumber 4615-69-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,1 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4615-69:
(6*4)+(5*6)+(4*1)+(3*5)+(2*6)+(1*9)=94
94 % 10 = 4
So 4615-69-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3O3/c1-5-9-7-3-2-6(11(13)14)4-8(7)10(5)12/h2-4,12H,1H3
4615-69-4Relevant articles and documents
From N-(dinitrophenyl) amino acids to benzimidazole N-oxides. Synthesis, kinetics and mechanism
Bujan, Elba I.,Salum, Maria Laura
, p. 187 - 195 (2006)
Several benzimidazole N-oxide derivatives were synthesized in very good yields by heating under reflux the corresponding N-(2,4- or 2,6-dinitrophenyl) amino acid derivative with NaOH in 60% 1,4-dioxane-H2O. The N-oxides obtained from glycine and α- and β-alanine derivatives lost the carboxylic group. The observed rate constant for the reaction of N-(2,4-dinitrophenyl) glycine (2a) in 10% 1,4-dioxane-H2O to give 5-nitro-1H-benzimidazole-3-oxide (4a) is first order on [NaOH]; the second-order rate constant is kN=1.7 × 10-3 M-1 S-1. The mechanism proposed includes the formation of an N-alkylidene 2-nitrosoaniline-type intermediate as the rate-determining step. Copyright
