CAS 1072946-66-7

Boronicacid, B-(6-chloro-5-fluoro-3-pyridinyl)-

Description:

Boronic acid derivatives, such as B-(6-chloro-5-fluoro-3-pyridinyl)-, are characterized by the presence of a boron atom bonded to a hydroxyl group and an organic substituent, in this case, a pyridine ring with specific halogen substitutions. This compound features a pyridine moiety that is substituted with both chlorine and fluorine atoms, which can influence its reactivity and biological activity. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including drug development and materials science. The presence of halogens can enhance the compound's lipophilicity and alter its electronic properties, potentially affecting its interaction with biological targets. Additionally, the structural features of this compound may contribute to its role in medicinal chemistry, particularly in the design of inhibitors or modulators for specific enzymatic pathways. Overall, the unique combination of boron chemistry and halogenated pyridine structures provides a versatile platform for further exploration in synthetic and pharmaceutical chemistry.

Formula: C₅H₄BClFNO₂

Synonyms:

• 2-Chloro-3-fluoropyridine-5-boronic acid

2-CHLORO-3-FLUOROPYRIDINE-5-BORONIC ACID

CAS: 1072946-66-7

Formula: C₅H₄BClFNO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 175.3532

Ref: IN-DA003BYV

2-Chloro-3-fluoropyridine-5-boronic acid

CAS: 1072946-66-7

2-Chloro-3-fluoropyridine-5-boronic acid

Purity: 97%

Molecular weight: 175.35g/mol

Ref: 54-PC3616

(6-Chloro-5-fluoropyridin-3-yl)boronic acid

CAS: 1072946-66-7

Formula: C₅H₄BClFNO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 175.35

Ref: 10-F222624