101079
3-溴苯酚
98%
别名:
m-Bromophenol
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关于此项目
线性分子式:
BrC6H4OH
化学文摘社编号:
分子量:
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
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.)
Quality Level
Gene Information
human ... ALOX12(239), ALOX15(246)
functional group
bromo
General description
3-溴苯酚用于suzuki-miyaura偶联反应，以及合成五环合成砌块苯并苯二苯并呋喃。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
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
法规信息
危险化学品
此项目有
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)
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
G F Rush et al.
Toxicology, 30(3), 259-272 (1984-04-02)
Bromobenzene, at doses greater than 5.7 mmol/kg, produced renal proximal tubular necrosis and renal functional changes in mice. p-Bromophenol and o-bromophenol were the major urinary phenolic bromobenzene metabolites although m-bromophenol and 4-bromocatechol were also excreted in detectable quantities. With the
S Chakrabarti et al.
Environmental research, 39(1), 50-59 (1986-02-01)
When male Sprague-Dawley rats were treated with 1 mg mercuric chloride (HgCl2)/kg, sc 6 hr prior to or simultaneously with a single 2.5-mmole/kg ip dose of bromobenzene and sacrificed 48 hr after the bromobenzene dose, the activities of serum transaminases
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