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101079

Sigma-Aldrich

3-Bromophenol

98%

Synonym(s):

m-Bromophenol

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About This Item

Linear Formula:
BrC6H4OH
CAS Number:
591-20-8
Molecular Weight:
173.01
Beilstein:
1853950
EC Number:
209-706-5
MDL number:
MFCD00002253
UNSPSC Code:
12352100
PubChem Substance ID:
24846532
NACRES:
NA.22

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

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

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General description

3-Bromophenol is used for suzuki-miyaura coupling reaction and in the synthesis of pentacyclic building block benzodibenzofuranquinone.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

No data available

Flash Point(C)

No data available

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
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
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.
R G Schnellmann et al.
The Journal of pharmacology and experimental therapeutics, 237(2), 456-461 (1986-05-01)
An in vitro model using a suspension of rabbit renal proximal tubules was developed to investigate the mechanism of nephrotoxicity of bromobenzene. Using oxygen consumption, glutathione concentrations and retention of lactate dehydrogenase activity as markers of toxicity, the rank order
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