Skip to Content
Merck
CN

281999

4-Bromobiphenyl

98%

Synonym(s):

(4-Bromophenyl)benzene, 1-Bromo-4-phenylbenzene, 4-Biphenyl bromide, 4′-Bromobiphenyl, p-Phenylphenyl bromide

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
C6H5C6H4Br
CAS Number:
Molecular Weight:
233.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-176-6
Beilstein/REAXYS Number:
1907453
MDL number:
Assay:
98%
Form:
solid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


Quality Level

assay

98%

form

solid

bp

310 °C (lit.)

mp

82-86 °C (lit.)

functional group

bromo, phenyl

SMILES string

Brc1ccc(cc1)-c2ccccc2

InChI

1S/C12H9Br/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H

InChI key

PKJBWOWQJHHAHG-UHFFFAOYSA-N

General description

In vitro metabolism of 4-bromobiphenyl by cytochrome P-450-dependent monooxygenases in rat hepatic microsomes has been investigated. 4-Bromobiphenyl undergoes reduction to biphenyl in cationic micelles (cetyltrimethyl-ammonium bromide) by electrochemically generated anion radicals of 9-phenylanthracene.

Application

4-Bromobiphenyl was used in the synthesis of 4-biphenylthiolate.


Still not finding the right product?

Explore all of our products under 4-Bromobiphenyl


signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



Structure of 4-biphenylthiolate on Au nanoparticle surfaces studied by UV-Vis absorption spectroscopy, transmission electron microscopy and surface-enhanced Raman scattering.
Jang S, et al.
Surface and Interface Analysis : SIA, 36(1), 43-48 (2004)
Electrocatalytic reactions in organized assemblies: Part I. Reduction of 4-bromobiphenyl in cationic and non-ionic micelles.
Rusling JF, et al.
J. Electroanal. Chem. Interfac. Electrochem., 240(1), 201-216 (1988)
A D Davison et al.
Canadian journal of microbiology, 42(1), 66-71 (1996-01-01)
Sphingomonas paucimobilis BPSI-3 was previously isolated from a mixed microbial consortium growing on biphenyl as the sole source of carbon and energy. Transformation of 4-chlorobiphenyl (4CBP) was demonstrated by this strain, although little or no growth was observed. In minimal



Global Trade Item Number

SKUGTIN
281999-10G04061826225783
281999-50G04061826226018