1039325-60-4 Usage
Description
1-(2-bromophenyl)-1H-1,2,3-triazole-4-carboxylic acid is a chemical compound characterized by the molecular formula C9H6BrN3O2. It is a derivative of the triazole class, featuring a carboxylic acid group and a bromophenyl substituent. 1-(2-bromophenyl)-1H-1,2,3-triazole-4-carboxylic acid is recognized for its potential in medicinal chemistry and drug development, serving as a versatile scaffold for the synthesis of bioactive compounds. Its unique structural and electronic properties also make it a subject of interest in organic chemistry research. Furthermore, it holds promise for applications in the fields of agrochemicals and materials science.
Uses
Used in Medicinal Chemistry and Drug Development:
1-(2-bromophenyl)-1H-1,2,3-triazole-4-carboxylic acid is used as a chemical scaffold for the synthesis of bioactive compounds. Its structural and electronic properties make it a valuable starting point for the development of new pharmaceuticals, potentially leading to the creation of novel therapeutic agents.
Used in Organic Chemistry Research:
In the field of organic chemistry, 1-(2-bromophenyl)-1H-1,2,3-triazole-4-carboxylic acid is used as a subject of study to explore its unique structural and electronic properties. This research can contribute to the understanding of triazole derivatives and their potential applications in various chemical processes.
Used in Agrochemical Development:
1-(2-bromophenyl)-1H-1,2,3-triazole-4-carboxylic acid is used as a potential component in the development of agrochemicals. Its properties may contribute to the creation of new compounds that can be utilized in agriculture for pest control, crop protection, or other related applications.
Used in Materials Science:
In materials science, 1-(2-bromophenyl)-1H-1,2,3-triazole-4-carboxylic acid is used for its potential to contribute to the development of new materials. Its unique properties may be harnessed to create innovative materials with specific characteristics, such as improved strength, durability, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 1039325-60-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,9,3,2 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1039325-60:
(9*1)+(8*0)+(7*3)+(6*9)+(5*3)+(4*2)+(3*5)+(2*6)+(1*0)=134
134 % 10 = 4
So 1039325-60-4 is a valid CAS Registry Number.
1039325-60-4Relevant articles and documents
One-Pot Synthesis of 1-Monosubstituted 1,2,3-Triazoles from Propargyl Alcohol
Han, Chunmei,Dong, Suping,Zhang, Wensheng,Chen, Zhen
, p. 673 - 677 (2018)
A one-pot synthesis of 1-monosubstituted-1,2,3-triazoles from propargyl alcohol and various aryl azides was achieved. This simple method provides concise and efficient access to various 1-monosubstituted 1,2,3-triazole derivatives through a three-step one
