CAS 2121512-87-4: B-[3-Chloro-5-(hydroxymethyl)phenyl]boronic acid

Description: B-[3-Chloro-5-(hydroxymethyl)phenyl]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 and other nucleophiles. This compound features a chlorinated phenyl ring, which enhances its reactivity and potential applications in organic synthesis and medicinal chemistry. The hydroxymethyl group contributes to its solubility in polar solvents and can participate in hydrogen bonding, influencing its interactions in biological systems. Boronic acids are often utilized in Suzuki coupling reactions, making this compound valuable in the synthesis of complex organic molecules. Additionally, the presence of the chlorine atom may impart unique electronic properties, affecting the compound's reactivity and stability. Overall, B-[3-Chloro-5-(hydroxymethyl)phenyl]boronic acid is a versatile building block in chemical research, particularly in the development of pharmaceuticals and agrochemicals.

Formula: C₇H₈BClO₃

InChI: InChI=1S/C7H8BClO3/c9-7-2-5(4-10)1-6(3-7)8(11)12/h1-3,10-12H,4H2

InChI key: InChIKey=GAIOEGMKZDBACM-UHFFFAOYSA-N

SMILES: ClC=1C=C(C=C(C1)CO)B(O)O

Synonyms:

• B-[3-Chloro-5-(hydroxymethyl)phenyl]boronic acid
• Boronic acid, B-[3-chloro-5-(hydroxymethyl)phenyl]-

3-Chloro-5-(hydroxymethyl)phenylboronic acid

CAS: 2121512-87-4

• Formula: C₇H₈BClO₃
• Purity: 97%
• Color and Shape: Solid
• Molecular weight: 186.4006

3-Chloro-5-(hydroxymethyl)phenylboronic acid

CAS: 2121512-87-4

• Purity: 96%
• Molecular weight: 186.40g/mol

(3-Chloro-5-(hydroxymethyl)phenyl)boronic acid

CAS: 2121512-87-4

• Purity: 97%
• Molecular weight: 186.39999389648438

3-Chloro-5-(hydroxymethyl)phenylboronic acid

CAS: 2121512-87-4

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• Formula: C₇H₈BClO₃
• Purity: Min. 95%
• Molecular weight: 186.4 g/mol