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2-(Bromomethyl)phenylboronic acid

ALDRICH/679453

Synonym: α-Bromo-o-tolueneboronic acid; o-Boronobenzyl bromide

CAS Number: 91983-14-1
Empirical Formula (Hill Notation): C7H8BBrO2
Molecular Weight: 214.85
MDL Number: MFCD01318941
Linear Formula: C7H8BBrO2
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-679453-1G 1 g
 $35.50
1/EA		 Add To Favorites
45-679453-5G 5 g
 $168.00
1/EA		 Add To Favorites
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 679453-1G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 679453-5G

 

functional group bromo
InChI 1S/C7H8BBrO2/c9-5-6-3-1-2-4-7(6)8(10)11/h1-4,10-11H,5H2
InChI key MYVJCOQGXCONPE-UHFFFAOYSA-N
mp 158-162 °C
Quality Level 100 
SMILES string OB(O)c1ccccc1CBr
storage temp. 2-8°C
Application: 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.
Application: 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 
General description: May contain varying amounts of anhydride.
Packaging: 1, 5 g in glass bottle
mp 158-162 °C
Storage Temp. 2-8°C
UNSPSC 12352103

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