2-(Bromomethyl)phenylboronic Acid

2-(Bromomethyl)phenylboronic acid can be used as a reactant to synthesize: Boronic acid-functionalized benzyl viologen (o-BBV) from 4,4'-bipyridine. o-BBV finds its application as a chemosensor to sense glucose in aqueous water; 2-(azidomethyl)phenylboronic acid, which is further employed in the preparation of isoquinoline derivatives.; Aryl boronic acid derivatives as fluorescent probe for hydrogen peroxide detection. Reactant involved in: Studies of carbon-boron bond cleavage of phenylboronate-pendant cyclen; Development of a sensory system to detect glucose or other monosaccharides and hydroxycarboxylates; Synthesis of boronated triaryl and tetraaryl phosphonium salts used in cytotoxicity studies; Colorimetry and fluorometry mercury determination with chemosensors composed of rhodamine and boronic acid groups; Synthesis of imidazolium-containing boronic acids used as fluoride ion sensors; Reactions with adenine for molecules with antiinflammatory antitumor activities.

[2-(bromomethyl)phenyl]boronic acid; [2-(bromomethyl)phenyl]boronic acid

[2-(bromomethyl)phenyl]boronic acid

B(C1=CC=CC=C1CBr)(O)O

InChI=1S/C7H8BBrO2/c9-5-6-3-1-2-4-7(6)8(10)11/h1-4,10-11H,5H2

MYVJCOQGXCONPE-UHFFFAOYSA-N

358.5 ℃ at 760 mmHg

158-162 ℃

Not applicable

1.57 g/cm³

2-8 ℃

0.26130

H315 - H319 - H335

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501

Warning