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:
产品名称
3-溴苯酚, 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)
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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
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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
Girish Chandra et al.
Archives of pharmacal research, 35(4), 639-645 (2012-05-04)
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