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679437

Sigma-Aldrich

4-(Bromomethyl)phenylboronic acid

Synonym(s):

α-Bromo-p-tolueneboronic acid, p-Boronobenzyl bromide

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About This Item

Linear Formula:
BrCH2(C6H4)B(OH)2
CAS Number:
68162-47-0
Molecular Weight:
214.85
MDL number:
MFCD01318113
UNSPSC Code:
12352103
PubChem Substance ID:
24885493
NACRES:
NA.22

form

solid

Quality Level

100

mp

173-177 °C

storage temp.

2-8°C

SMILES string

OB(O)c1ccc(CBr)cc1

InChI

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

InChI key

PDNOURKEZJZJNZ-UHFFFAOYSA-N

General description

May contain varying amounts of anhydride

Application

Reactant involved in:
  • Design of boronic acid-based autotaxin inhibitors
  • Synthesis of boronated phosphonium salts
  • Studies of incorporation of boronic acid groups to enhance gene transfection capability
  • Investigations of the effect of boronic acid-positioning in optical glucose-sensing ensemble

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Chongyi Liu et al.
Advanced healthcare materials, 5(5), 584-592 (2016-01-21)
Cationic dendrimers are widely used as nonviral gene vectors, however, current gene materials based on dendrimers are either little effective or too toxic on the transfected cells. Here, a facile strategy is presented to prepare high efficient dendrimers with low

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