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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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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.
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
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
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