CAS 951655-49-5

(2-oxo-1,2-dihydropyridin-3-yl)boronic acid

Description:

(2-Oxo-1,2-dihydropyridin-3-yl)boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a hydroxyl group and a pyridine-like structure. This compound features a dihydropyridine ring with a ketone functional group at the 2-position, which contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. The boronic acid functionality allows for the formation of reversible covalent bonds with diols, making it useful in various chemical reactions, including Suzuki coupling reactions, which are pivotal in the synthesis of biaryl compounds. Additionally, the presence of the oxo group enhances its electrophilic character, potentially increasing its reactivity in nucleophilic addition reactions. This compound may also exhibit biological activity, making it of interest in drug development and research. Its solubility and stability in different solvents can vary, influencing its practical applications in laboratory settings. Overall, (2-oxo-1,2-dihydropyridin-3-yl)boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.

(2-Hydroxypyridin-3-yl)boronic acid

CAS: 951655-49-5

Formula: C₅H₆BNO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 138.9170

Ref: IN-DA00IISK

(2-Oxo-1,2-dihydropyridin-3-yl)boronic acid

CAS: 951655-49-5

(2-Oxo-1,2-dihydropyridin-3-yl)boronic acid

Formula: C₅H₆BNO₃

Purity: >95% (nmr) (Typical Value in Batch COA)

Color and Shape: pale yellow powder

Molecular weight: 138.92g/mol

Ref: 54-OR302583

(2-Oxo-1,2-dihydropyridin-3-yl)boronic acid

CAS: 951655-49-5

Formula: C₅H₆BNO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 138.92

Ref: 10-F318171

2-Oxo-1,2-dihydropyridin-3-yl-boronic Acid

Controlled Product

CAS: 951655-49-5

Formula: C₅H₆BNO₃

Color and Shape: Neat

Molecular weight: 138.917

Ref: TR-O855300