132543
4-溴丁基苯基醚
97%
别名:
4-苯氧基丁基溴, 4-苯氧基溴丁烷, 苯氧基丁基溴
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关于此项目
线性分子式:
C6H5OCH2CH2CH2CH2Br
化学文摘社编号:
分子量:
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.)
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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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