Sign In to View Organizational & Contract Pricing
Select a Size
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
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
human ... ALOX12(239), ALOX15(246)
Looking for similar products? Visit Product Comparison Guide
Related Categories
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.
Signal Word
Warning
Hazard Statements
Precautionary 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
Regulatory Information
危险化学品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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)
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)
Cyclodextrin-derived diorganyl tellurides as glutathione peroxidase mimics and inhibitors of thioredoxin reductase and cancer cell growth.
McNaughton M, et al.
Journal of Medicinal Chemistry, 47(1), 233-239 (2004)
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)
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)
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