Skip to Content
Merck
All Photos(4)

Documents

B75808

Sigma-Aldrich

4-Bromophenol

99%

Synonym(s):

1-Bromo-4-hydroxybenzene, p-Bromophenol

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
BrC6H4OH
CAS Number:
Molecular Weight:
173.01
Beilstein:
1680024
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

solid

bp

235-236 °C (lit.)

mp

61-64 °C (lit.)

SMILES string

Oc1ccc(Br)cc1

InChI

1S/C6H5BrO/c7-5-1-3-6(8)4-2-5/h1-4,8H

InChI key

GZFGOTFRPZRKDS-UHFFFAOYSA-N

Gene Information

Looking for similar products? Visit Product Comparison Guide

Application

4-Bromophenol is a common aryl bromide reagent that can be used in various cross-coupling reactions to synthesize compounds for medicinal and material science applications.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Amphiphilic diarylethene as a photoswitchable probe for imaging living cells.
Zou Y, et al.
Journal of the American Chemical Society, 130(47), 15750-15751 (2008)
Versatile catalysts for the Suzuki cross-coupling of arylboronic acids with aryl and vinyl halides and triflates under mild conditions.
Littke A F, et al.
Journal of the American Chemical Society, 122(17), 4020-4028 (2000)
Dendrimer-encapsulated Pd nanoparticles as aqueous, room-temperature catalysts for the Stille reaction.
Garcia-Martinez J C, et al.
Journal of the American Chemical Society, 127(14), 5097-5103 (2005)
A versatile catalyst for Heck reactions of aryl chlorides and aryl bromides under mild conditions.
Littke A F and Fu G C
Journal of the American Chemical Society, 123(29), 6989-7000 (2001)
Live-cell one-and two-photon uncaging of a far-red emitting acridinone fluorophore.
Warther D, et al.
Journal of the American Chemical Society, 132(8), 2585-2590 (2010)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service