18000
3-Bromophenol
purum, ≥97.5% (HPLC)
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About This Item
Linear Formula:
BrC6H4OH
CAS Number:
Molecular Weight:
173.01
EC Number:
209-706-5
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1853950
MDL number:
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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
grade
purum
assay
≥97.5% (HPLC)
bp
236 °C (lit.)
Gene Information
human ... ALOX12(239), ALOX15(246)
mp
28-32 °C
solubility
alcohol: soluble, diethyl ether: soluble
Application
3-Bromophenol was used in the synthesis of 3-lithium-o-lithiophenoxide.
Disclaimer
may form a subcooled melt
comparable product
Product No.
Description
Pricing
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
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
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Samira Islas-Valdez et al.
International journal of biological macromolecules, 142, 163-171 (2019-09-17)
Lignosulfonates (LSs) are by-products from the paper industry used as biodegradable fertilizers. However, metal-LS ability to provide micronutrients to crops is related to the stability of the complex and the amount of metal complexed. This work evaluated these parameters using
Theodore N Djeni et al.
Scientific reports, 10(1), 1715-1715 (2020-02-06)
Palm wine, the most commonly consumed traditional alcoholic beverage in Western Africa, harbours a complex microbiota and metabolites, which plays a crucial role in the overall quality and value of the product. In the present study, a combined metagenomic and
Preparation and trapping of 3-lithium-O-lithiophenoxide.
Tetrahedron Letters, 34(13), 2043-2046 (1993)
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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