679437
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:
Molecular Weight:
214.85
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
form
solid
Quality Level
mp
173-177 °C
functional group
bromo
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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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