3-(Hydroxymethyl)phenylboronic acid

3-(Hydroxymethyl)phenylboronic acid Basic information

Product Name:	3-(Hydroxymethyl)phenylboronic acid
Synonyms:	RARECHEM AH PB 0189;3-(HYDROXYMETHYL)PHENYLBORONIC ACID;3-(HYDROXYMETHYL)BENZENEBORONIC ACID;(3-Boronophenyl)methanol;3-Boronobenzyl alcohol;3-(Hydroxymethyl)phenylboronic Acid (contains varying amounts of Anhydride);3-(Hydroxymethyl)phenylboronic acid,97%;3-hydroxymethylboronic acid
CAS:	87199-15-3
MF:	C7H9BO3
MW:	151.96
EINECS:
Product Categories:	Boronic Acid;B (Classes of Boron Compounds);blocks;Aryl;Organoborons;Boronic Acids;BoronicAcids;Boric Acid;Boronic Acid series;Boronic Acids;Boronic Acids and Derivatives
Mol File:	87199-15-3.mol

3-(Hydroxymethyl)phenylboronic acid Chemical Properties

Melting point	95-99 °C (lit.)
Boiling point	380.5±44.0 °C(Predicted)
density	1.25±0.1 g/cm3(Predicted)
storage temp.	Keep in dark place,Sealed in dry,Room Temperature
pka	8.31±0.10(Predicted)
form	powder to crystal
color	White to Almost white
Water Solubility	Soluble in water.
BRN	8832019
CAS DataBase Reference	87199-15-3(CAS DataBase Reference)

Safety Information

MSDS Information

3-(Hydroxymethyl)phenylboronic acid Usage And Synthesis

Chemical Properties	Off-white Cryst
Uses	suzuki reaction
Uses	Reactant used for copper-mediated trifluoromethylation, copper-catalyzed transformations from arylboronic acids in water, Mitsunobu, Suzuki, and amidation reactions with hydroxyphenylamino bromopyrazinecarboxylate. Reactant involved in the synthesis of biologically active molecules including Mycobacterium tuberculosis H37Rv chorismate mutase inhibitors via Suzuki coupling reactions, HIV protease inhibitors with antiviral activity against drug-resistant viruses, Pyrrole derivatives for use as PDE4B inhibitors.

3-(Hydroxymethyl)phenylboronic acid Preparation Products And Raw materials

Preparation Products

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