162356-38-9 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
2-(2-Bromo-phenyl)-1H-imidazole is used as a building block for creating other organic compounds, particularly in the synthesis of biologically active compounds. Its unique structure and reactivity contribute to the development of new pharmaceutical agents with potential therapeutic applications.
Used in Organic Chemistry and Chemical Research:
In the field of organic chemistry, 2-(2-Bromo-phenyl)-1H-imidazole serves as an important reagent, facilitating the synthesis of a wide range of chemical compounds. Its presence in various chemical reactions enhances the exploration of new chemical pathways and the discovery of novel materials with specific properties.
Used in the Synthesis of Materials:
2-(2-Bromo-phenyl)-1H-imidazole is utilized in the synthesis of materials with unique properties, such as those with enhanced stability, reactivity, or selectivity. Its incorporation into material compositions can lead to advancements in various industries, including electronics, coatings, and specialty chemicals.
Used in Chemical Industry:
In the chemical industry, 2-(2-Bromo-phenyl)-1H-imidazole is employed for its potential applications in the production of intermediates and specialty chemicals. Its unique properties can be leveraged to create new products or improve existing processes, contributing to innovation and efficiency in chemical manufacturing.
Check Digit Verification of cas no
The CAS Registry Mumber 162356-38-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,3,5 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 162356-38:
(8*1)+(7*6)+(6*2)+(5*3)+(4*5)+(3*6)+(2*3)+(1*8)=129
129 % 10 = 9
So 162356-38-9 is a valid CAS Registry Number.
162356-38-9Relevant academic research and scientific papers
Catalytic Activation of Cis-Vicinal Diols by Boronic Acids: Site-Selective Acylation of Carbohydrates
Shimada, Naoyuki,Nakamura, Yuki,Ochiai, Takayuki,Makino, Kazuishi
supporting information, p. 3789 - 3794 (2019/05/24)
Site-selective acylation of unprotected carbohydrates by using stable, storable, and easily handled imidazole-containing organoboronic acid catalysts is described. This catalytic process with low catalyst loading enables the introduction of a wide variety of acyl functional groups into the equatorial position of cis-vicinal diols in unprotected hexapyranosides with excellent site selectivity. This is the first example that uses a Lewis base-containing boronic acid to enhance the nucleophilicity of hydroxy groups.
