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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:
Molecular Weight:
214.85
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

form

solid

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

Related Categories

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

Signal Word

Warning

Hazard 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

Certificates of Analysis (COA)

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Ding Ma et al.
ACS applied materials & interfaces, 12(8), 9032-9040 (2020-01-28)
MicroRNAs (miRNAs) therapy has shown to have great promise for the treatment of androgen-independent prostate cancer (AIPC) due to the low efficiency of hormonal therapy. However, instability of RNA and inefficiency of RNA therapy limit the use of miRNAs in
Yu-Lin Su et al.
Journal of controlled release : official journal of the Controlled Release Society, 321, 159-173 (2020-02-12)
Compact nanohybrids can potentially unite various therapeutic features and reduce side effects for precise cancer therapy. However, the poor accumulation and limited tumor penetration of drugs at the tumor impede the manifestation of nanomedicine. We developed a rabies virus glycoprotein
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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