All Photos(1)
(4-Bromobutoxy)benzene, 4-Phenoxybutyl bromide, Phenoxybutyl bromide
C6H5OCH2CH2CH2CH2Br
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Assay
97%
form
solid
bp
153-156 °C/18 mmHg (lit.)
mp
41-43 °C (lit.)
SMILES string
BrCCCCOc1ccccc1
InChI
1S/C10H13BrO/c11-8-4-5-9-12-10-6-2-1-3-7-10/h1-3,6-7H,4-5,8-9H2
InChI key
QBLISOIWPZSVIK-UHFFFAOYSA-N
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WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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.
Journal of Electroanalytical Chemistry, 380(1), 147-160 (1995)
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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