101079
3-Bromophenol
98%
Synonym(s):
m-Bromophenol
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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:
Assay:
98%
Form:
solid
Quality Segment
assay
98%
form
solid
bp
236 °C (lit.)
mp
28-32 °C (lit.)
functional group
bromo
SMILES string
Oc1cccc(Br)c1
InChI
1S/C6H5BrO/c7-5-2-1-3-6(8)4-5/h1-4,8H
InChI key
MNOJRWOWILAHAV-UHFFFAOYSA-N
Gene Information
human ... ALOX12(239), ALOX15(246)
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
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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)
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)
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 101079-10G | 04061838666864 |
| 101079-25G | 04061838666871 |
| 101079-100G | 04061838344731 |