CAS 1451391-54-0: 3-​Hydroxymethyl-​4-​methylphenylboronic acid

Description: 3-Hydroxymethyl-4-methylphenylboronic 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. This compound features a hydroxymethyl group and a methyl group attached to a phenyl ring, contributing to its unique reactivity and solubility properties. It is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, making it useful in various chemical applications. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. Additionally, this compound may exhibit biological activity, making it of interest in medicinal chemistry. Its stability and reactivity can be influenced by pH and the presence of other functional groups, which is crucial for its application in synthetic pathways and potential therapeutic uses. Overall, 3-hydroxymethyl-4-methylphenylboronic acid is a versatile compound with significant implications in both organic synthesis and pharmaceutical development.

Boronic acid, B-[3-(hydroxymethyl)-4-methylphenyl]-

CAS: 1451391-54-0

• Formula: C₈H₁₁BO₃
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 165.9821

3-Hydroxymethyl-4-methylphenylboronic acid

CAS: 1451391-54-0

• Purity: 98%
• Molecular weight: 165.98g/mol

3-(Hydroxymethyl)-4-methylphenylboronic acid

CAS: 1451391-54-0

• Purity: 97%
• Molecular weight: 165.982

(3-(Hydroxymethyl)-4-methylphenyl)boronic acid

CAS: 1451391-54-0

• Purity: 95.0%
• Molecular weight: 165.97999572753906

3-Hydroxymethyl-4-methylphenylboronic acid

CAS: 1451391-54-0

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• Formula: C₈H₁₁BO₃
• Purity: Min. 95%
• Molecular weight: 165.98 g/mol