Boronic acid, specifically B-(5-chloro-2-methyl-3-nitrophenyl)-, is an organoboron compound characterized by the presence of a boron atom bonded to a phenyl group that contains various substituents. This compound typically features a boronic acid functional group (-B(OH)2), which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the 5-chloro, 2-methyl, and 3-nitro substituents on the phenyl ring contributes to its unique reactivity and properties, influencing its electronic characteristics and solubility. Boronic acids are often utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the nitro group can enhance the compound's electrophilicity, while the chloro and methyl groups can affect steric hindrance and overall molecular stability. Overall, this compound exemplifies the versatility of boronic acids in synthetic organic chemistry.

Boronic acid,B-(5-chloro-2-methyl-3-nitrophenyl)-

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(5-Chloro-2-methyl-3-nitrophenyl)boronic acid

5-Chloro-2-methyl-3-nitrobenzeneboronic acid

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CAS 957060-80-9: Boronic acid,B-(5-chloro-2-methyl-3-nitrophenyl)-

(5-Chloro-2-methyl-3-nitrophenyl)boronic acid

Ref: IN-DA00H843

5-Chloro-2-methyl-3-nitrobenzeneboronic acid

Ref: 54-OR3499

5-Chloro-2-methyl-3-nitrobenzeneboronic acid

Ref: 3D-HNB06080