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132543

Sigma-Aldrich

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:
1200-03-9
Molecular Weight:
229.11
EC Number:
214-849-1
MDL number:
MFCD00000262
UNSPSC Code:
12352100
PubChem Substance ID:
24848058
NACRES:
NA.22

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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Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBP4748V
14322CH
13211AH
04229HE
07022KD

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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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