20223-87-4 Usage
Uses
Used in Pharmaceutical Synthesis:
4-BROMO-2-METHYL-1H-BENZIMIDAZOLE is used as a key intermediate in the synthesis of pharmaceuticals for its potential role in the development of new drugs. Its unique structure allows for the creation of compounds with therapeutic properties, making it valuable in medicinal chemistry.
Used in Agrochemical Production:
In the agrochemical industry, 4-BROMO-2-METHYL-1H-BENZIMIDAZOLE is utilized as a building block in the synthesis of various agrochemicals, contributing to the development of effective and targeted pest control solutions.
Used in Organic Material Development:
This benzimidazole derivative is employed as a component in the development of organic materials, where its chemical properties can enhance the performance of these materials in different applications.
Used in Dye Manufacturing:
4-BROMO-2-METHYL-1H-BENZIMIDAZOLE is used as a precursor in dye manufacturing, where its chemical structure contributes to the color and stability of the resulting dyes, suitable for various industrial uses.
Overall, 4-BROMO-2-METHYL-1H-BENZIMIDAZOLE is a significant intermediate in the production of a variety of compounds with potential applications across multiple industries, including pharmaceuticals, agrochemicals, organic materials, and dyes.
Check Digit Verification of cas no
The CAS Registry Mumber 20223-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,2 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20223-87:
(7*2)+(6*0)+(5*2)+(4*2)+(3*3)+(2*8)+(1*7)=64
64 % 10 = 4
So 20223-87-4 is a valid CAS Registry Number.
20223-87-4Relevant academic research and scientific papers
Novel strategy for synthesis of substituted benzimidazo[1,2-a]quinolines
Kato, Jun-Ya,Ito, Yutaro,Ijuin, Ryosuke,Aoyama, Hiroshi,Yokomatsu, Tsutomu
supporting information, p. 3794 - 3797 (2013/08/23)
An efficient method for the synthesis of benzimidazo[1,2-a]quinolines under transition-metal-free conditions has been developed through a cascade reaction involving sequential aromatic nucleophilic substitution and intramolecular Knoevenagel condensation reactions. This method is applicable for the synthesis of a wide range of benzimidazo[1,2-a]quinoline derivatives from readily available 2-fluoroarylaldehyde and benzimidazole substrates.
Synthesis of heterocyclic aza-phosphinate ligands based on the benzimidazole skeleton
Edlin, Chris D.,Parker, David
, p. 2797 - 2800 (2007/10/03)
Three new heterocyclic ligand systems based on the benzimidazole ring system have been designed and synthesised. These ligands have been prepared with a view to the selective coordination of zinc ions in a tetrahedral environment.
