(2-Chloro-4-methoxy-5-methoxycarbonyl-phenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, 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 compound features a phenyl ring substituted with a chlorine atom, two methoxy groups, and a methoxycarbonyl group, contributing to its unique reactivity and solubility properties. The presence of the boronic acid moiety allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, the methoxy and methoxycarbonyl substituents can influence the electronic properties of the molecule, potentially enhancing its reactivity or selectivity in chemical reactions. This compound may also exhibit interesting biological activities, making it a candidate for further research in drug development. Overall, its structural features and functional groups make it a versatile compound in both synthetic and pharmaceutical chemistry.

(2-chloro-4-methoxy-5-methoxycarbonyl-phenyl)boronic acid

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CAS 957066-07-8: (2-chloro-4-methoxy-5-methoxycarbonyl-phenyl)boronic acid

2-Chloro-4-methoxy-5-(methoxycarbonyl)benzeneboronic acid

Ref: 3D-HNB06607

(2-Chloro-4-methoxy-5-(methoxycarbonyl)phenyl)boronic acid

Ref: IN-DA003BMO

2-Chloro-4-methoxy-5-(methoxycarbonyl)benzeneboronic acid

Ref: 54-OR59416