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101079

Sigma-Aldrich

3-Bromophenol

98%

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Synonym(s):
m-Bromophenol
Linear Formula:
BrC6H4OH
CAS Number:
Molecular Weight:
173.01
Beilstein/REAXYS Number:
1853950
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

form

solid

bp

236 °C (lit.)

mp

28-32 °C (lit.)

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

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1 of 4

This Item
130915100242B75808
vibrant-m

101079

3-Bromophenol

vibrant-m

130915

2-Bromophenol

vibrant-m

100242

3-Aminophenol

vibrant-m

B75808

4-Bromophenol

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

200

mp

28-32 °C (lit.)

mp

3-7 °C (lit.)

mp

120-124 °C (lit.)

mp

61-64 °C (lit.)

bp

236 °C (lit.)

bp

195 °C (lit.)

bp

164 °C/11 mmHg (lit.)

bp

235-236 °C (lit.)

form

solid

form

liquid

form

solid

form

solid

Gene Information

human ... ALOX12(239), ALOX15(246)

Gene Information

human ... ALOX12(239), ALOX15(246)

Gene Information

-

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.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

No data available

flash_point_c

No data available

ppe

dust mask type N95 (US), Eyeshields, Gloves


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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)
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
D Mahadevan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(2), 575-581 (2010-12-28)
The FT-IR and FT-Raman spectra of 3-Bromo phenol (3-BP) molecule have been recorded using Bruker IFS 66V spectrometer in the range of 4000-100 cm(-1). The molecular geometry and vibrational frequencies in the ground state are calculated by using the ab

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