Boronic acid, specifically B-(2-bromo-3-chloro-4-pyridinyl)-, is an organoboron compound characterized by the presence of a boron atom bonded to a pyridine ring that is substituted with both bromine and chlorine atoms. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of halogen substituents can enhance its reactivity and influence its electronic properties, potentially making it a valuable intermediate in the synthesis of pharmaceuticals or agrochemicals. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds. The specific arrangement of substituents in this compound may also impart unique characteristics, such as solubility in organic solvents and varying degrees of acidity, which can be important for its reactivity in chemical reactions. Overall, this compound represents a versatile building block in synthetic organic chemistry.

Boronic acid,B-(2-bromo-3-chloro-4-pyridinyl)-

1003043-31-9: (2-Bromo-3-chloropyridin-4-yl)boronic acid,  boronic acid, B-(2-bromo-3-chloro-4-pyridinyl)-

2-Bromo-3-chloropyridine-4-boronic acid

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CAS 1003043-31-9: Boronic acid,B-(2-bromo-3-chloro-4-pyridinyl)-

2-Bromo-3-chloropyridine-4-boronic acid

Ref: 54-OR9502

2-Bromo-3-chloropyridine-4-boronicacid

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2-Bromo-3-chloropyridine-4-boronic acid

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Boronic acid, B-(2-bromo-3-chloro-4-pyridinyl)-

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