CAS 2096330-20-8: B-(2-Butoxy-5-methyl-3-pyridinyl)boronic acid

Description: B-(2-Butoxy-5-methyl-3-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound typically exhibits properties such as being a solid at room temperature, with potential solubility in polar organic solvents due to the presence of the butoxy group. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, which are valuable in organic synthesis for forming carbon-carbon bonds. The pyridine ring contributes to the compound's aromaticity and may influence its reactivity and interaction with biological systems. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be significant in biochemical applications. Overall, B-(2-Butoxy-5-methyl-3-pyridinyl)boronic acid is a versatile compound with potential applications in medicinal chemistry and materials science, owing to its unique structural features and reactivity.

Formula: C₁₀H₁₆BNO₃

InChI: InChI=1S/C10H16BNO3/c1-3-4-5-15-10-9(11(13)14)6-8(2)7-12-10/h6-7,13-14H,3-5H2,1-2H3

InChI key: InChIKey=CZLJBFIYFSIFEU-UHFFFAOYSA-N

SMILES: OB(O)C1=CC(=CN=C1OCCCC)C

Synonyms:

• Boronic acid, B-(2-butoxy-5-methyl-3-pyridinyl)-
• B-(2-Butoxy-5-methyl-3-pyridinyl)boronic acid

2-Butoxy-5-methylpyridine-3-boronic acid

CAS: 2096330-20-8

• Purity: 97%
• Molecular weight: 209.0500030517578

2-Butoxy-5-methylpyridine-3-boronic acid

CAS: 2096330-20-8

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• Formula: C₁₀H₁₆BNO₃
• Purity: Min. 95%
• Molecular weight: 209.05 g/mol