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Key Documents

132543

Sigma-Aldrich

4-溴丁基苯基醚

97%

同義詞:

4-苯氧基丁基溴, 4-苯氧基溴丁烷, 苯氧基丁基溴

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About This Item

線性公式:
C6H5OCH2CH2CH2CH2Br
CAS號碼:
分子量::
229.11
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

形狀

solid

bp

153-156 °C/18 mmHg (lit.)

mp

41-43 °C (lit.)

SMILES 字串

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 密鑰

QBLISOIWPZSVIK-UHFFFAOYSA-N

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儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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分析證明 (COA)

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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
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
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)

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