CAS 2096341-71-6: B-[3-Chloro-2-(1-methylethoxy)-4-pyridinyl]boronic acid

Description: B-[3-Chloro-2-(1-methylethoxy)-4-pyridinyl]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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a pyridine ring substituted with a chlorine atom and an ethoxy group, which contributes to its reactivity and solubility properties. The presence of the boronic acid moiety allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as boronic acids can act as enzyme inhibitors or serve as building blocks in organic synthesis. Additionally, the compound's structural features may influence its biological activity, making it a candidate for further investigation in drug discovery. Its specific physical and chemical properties, such as melting point, solubility, and stability, would typically be determined through experimental methods and may vary based on the conditions of use.

Formula: C₈H₁₁BClNO₃

InChI: InChI=1S/C8H11BClNO3/c1-5(2)14-8-7(10)6(9(12)13)3-4-11-8/h3-5,12-13H,1-2H3

InChI key: InChIKey=LTYSIEFEZIZESX-UHFFFAOYSA-N

SMILES: ClC=1C(=NC=CC1B(O)O)OC(C)C

Synonyms:

• Boronic acid, B-[3-chloro-2-(1-methylethoxy)-4-pyridinyl]-
• B-[3-Chloro-2-(1-methylethoxy)-4-pyridinyl]boronic acid

3-Chloro-2-isopropoxypyridine-4-boronic acid

CAS: 2096341-71-6

• Purity: 97%
• Molecular weight: 215.44000244140625

3-Chloro-2-isopropoxypyridine-4-boronic acid

CAS: 2096341-71-6

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• Formula: C₈H₁₁BClNO₃
• Purity: Min. 95%
• Molecular weight: 215.44 g/mol