2034-23-3 Usage
Description
5-CHLORO-1H-BENZOIMIDAZOL-2-OL, also known as 5-Chloro-2-benzimidazolinone, is an organic compound with the molecular formula C7H5ClN2O. It is a heterocyclic compound featuring a benzene ring fused to an imidazole ring, with a chlorine atom at the 5-position and a hydroxyl group at the 2-position. 5-CHLORO-1H-BENZOIMIDAZOL-2-OL is known for its potential applications in various fields due to its unique chemical structure and properties.
Uses
Used in Chemical Synthesis:
5-CHLORO-1H-BENZOIMIDAZOL-2-OL is used as an intermediate in the synthesis of various organic compounds, particularly those with pharmaceutical or chemical applications. Its unique structure allows for further functionalization and modification, making it a versatile building block in the development of new molecules.
Used in the Preparation of Photocatalysts:
In the field of materials science, 5-CHLORO-1H-BENZOIMIDAZOL-2-OL is used in the preparation of sea urchin-like cobalt-based photocatalysts. These photocatalysts are designed to enhance the efficiency of light-induced chemical reactions, such as the conversion of carbon dioxide into more valuable compounds.
Used in Carbon Dioxide Conversion:
5-CHLORO-1H-BENZOIMIDAZOL-2-OL plays a crucial role in the conversion of carbon dioxide (CO2) into benzoazepine derivatives. This process is of significant interest due to the potential for reducing greenhouse gas emissions and creating valuable chemicals from waste CO2. The compound's involvement in this process highlights its utility in environmental and sustainable chemistry applications.
Check Digit Verification of cas no
The CAS Registry Mumber 2034-23-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2034-23:
(6*2)+(5*0)+(4*3)+(3*4)+(2*2)+(1*3)=43
43 % 10 = 3
So 2034-23-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5ClN2O/c8-4-1-2-5-6(3-4)10-7(11)9-5/h1-3H,(H2,9,10,11)
2034-23-3Relevant articles and documents
Synthese de Nouvelles 4-Acetonylidene-1,5-benzodiazepin-2-ones III: Etude de la Reaction de Condensation des o-Phenylenediamines monosubstituees avec la γ-pyrone
Abbassi, M. El,Essassi, E. M.,Fifani, J.
, p. 205 - 210 (2007/10/03)
Condensation of unsymmetrical aromatic diamines (4-methyl-, 4-chloro-, and 4-nitrophenylenediamines) 2-4 with 2-hydroxy-6-methyl-4-pyrone 1 have been examinated. The structure of isomerie 4-acetonylidene-1,5-benzodiazepin-2-ones 5-10 and benzimidazoles 11-16 obtained from competitive reactions have been established by the spectrale data (1H NMR, IR and mass spectrum). The position of the substituents in 6/9 and 7/10 was proved by comparison with samples with authentic structures.
