101079
3-Bromophenol
98%
Synonym(s):
m-Bromophenol
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
BrC6H4OH
CAS Number:
Molecular Weight:
173.01
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-706-5
Beilstein/REAXYS Number:
1853950
MDL number:
Product Name
3-Bromophenol, 98%
InChI key
MNOJRWOWILAHAV-UHFFFAOYSA-N
InChI
1S/C6H5BrO/c7-5-2-1-3-6(8)4-5/h1-4,8H
SMILES string
Oc1cccc(Br)c1
assay
98%
form
solid
bp
236 °C (lit.)
mp
28-32 °C (lit.)
functional group
bromo
Quality Level
Gene Information
human ... ALOX12(239), ALOX15(246)
Looking for similar products? Visit Product Comparison Guide
Related Categories
General description
3-Bromophenol is used for suzuki-miyaura coupling reaction and in the synthesis of pentacyclic building block benzodibenzofuranquinone.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
No data available
flash_point_c
No data available
ppe
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.
Kesong Tian et al.
Nature communications, 11(1), 3884-3884 (2020-08-06)
Integrating nitrogen species into sp2-hybridized carbon materials has proved an efficient means to improve their electrochemical performance. Nevertheless, an inevitable mixture of nitrogen species in carbon materials, due to the uncontrolled conversion among different nitrogen configurations involved in synthesizing nitrogen-doped
Palladium loaded on ZnO nanoparticles: Synthesis, characterization and application as heterogeneous catalyst for Suzuki--Miyaura cross-coupling reactions under ambient and ligand-free conditions
Digambar B B et al.
Materials Chemistry and Physics, 243, 122561-122561 (2020)
Synthesis of a versatile pentacyclic building block for organic electronics
Brenden M et al.
Journal of Polymer Science Part A: Polymer Chemistry, 55, 2618-2628 (2017)
K Lertratanangkoon et al.
Drug metabolism and disposition: the biological fate of chemicals, 15(6), 857-867 (1987-11-01)
Premercapturic acids derived from bromobenzene 3,4-oxide were found to act as precursors of 3- and 4-bromophenol in the rat and guinea pig. The 4-S- and 3-S- positional isomers used in this study were rat urinary metabolites and were prepared in
Girish Chandra et al.
Archives of pharmacal research, 35(4), 639-645 (2012-05-04)
An improved synthesis of DNA-dependent protein kinase inhibitor, IC86621 is described. This developed method provides an easy access to this simple molecule by using amination, acetylation and Fries rearrangement reactions.
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