132543
4-Bromobutyl phenyl ether
97%
Synonym(s):
(4-Bromobutoxy)benzene, 4-Phenoxybutyl bromide, Phenoxybutyl bromide
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About This Item
Linear Formula:
C6H5OCH2CH2CH2CH2Br
CAS Number:
Molecular Weight:
229.11
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
214-849-1
MDL number:
Assay:
97%
Form:
solid
InChI key
QBLISOIWPZSVIK-UHFFFAOYSA-N
InChI
1S/C10H13BrO/c11-8-4-5-9-12-10-6-2-1-3-7-10/h1-3,6-7H,4-5,8-9H2
SMILES string
BrCCCCOc1ccccc1
assay
97%
form
solid
bp
153-156 °C/18 mmHg (lit.)
mp
41-43 °C (lit.)
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Jun Terao et al.
Chemistry, an Asian journal, 3(8-9), 1472-1478 (2008-07-10)
Regioselective double alkylation of styrenes with alkyl Grignard reagents and alkyl bromides having a heteroatom functional group at the beta-position has been achieved by the use of a titanocene catalyst in THF. When ether was used instead of THF as
Electrochemical reduction of 1, 4-dihalobutanes at carbon cathodes in dimethylformamide.
Pritts WA and Peters DG.
Journal of Electroanalytical Chemistry, 380(1), 147-160 (1995)
Johan R Johansson et al.
The Journal of organic chemistry, 76(7), 2355-2359 (2011-03-11)
An experimentally simple sequential one-pot RuAAC reaction, affording 1,5-disubstituted 1H-1,2,3-triazoles in good to excellent yields starting from an alkyl halide, sodium azide, and an alkyne, is reported. The organic azide is formed in situ by treating the primary alkyl halide
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