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CAS 1072946-45-2

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Boronic acid, B-[4-(aminomethyl)-3-fluorophenyl]-, hydrochloride (1:1)

Description:
Boronic acid, B-[4-(aminomethyl)-3-fluorophenyl]-, hydrochloride (1:1) is a chemical 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 fluorinated aromatic ring, specifically a 3-fluorophenyl group, which can influence its electronic properties and reactivity. The presence of the aminomethyl substituent enhances its potential for biological activity, making it of interest in medicinal chemistry. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, facilitating its use in various applications, including drug formulation and organic synthesis. The compound's structure allows for participation in Suzuki coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds. Overall, this boronic acid derivative exhibits unique characteristics that make it valuable in both research and pharmaceutical contexts, particularly in the development of targeted therapies and chemical probes.
Formula:C7H9BFNO2·ClH
InChI:InChI=1S/C7H9BFNO2.ClH/c9-7-3-6(8(11)12)2-1-5(7)4-10;/h1-3,11-12H,4,10H2;1H
InChI key:InChIKey=HOFYPLPXUYJZCR-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(F)=C(CN)C=C1.Cl
Synonyms:
  • Boronic acid, B-[4-(aminomethyl)-3-fluorophenyl]-, hydrochloride (1:1)
  • (4-(Aminomethyl)-3-fluorophenyl)boronic acid hydrochloride
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