(4-Bromobutoxy)benzene

Names

[ Name ]:
(4-Bromobutoxy)benzene

[Synonym ]:
Benzene, (4-bromobutoxy)-
4-Bromobutyl phenyl ether
4-bromobutoxybenzene
4-Brombutyl-phenylether
MFCD00000262
(4-Bromobutoxy)benzene
EINECS 214-849-1

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
282.3±0.0 °C at 760 mmHg

[ Melting Point ]:
41-43 °C(lit.)

[ Molecular Formula ]:
C₁₀H₁₃BrO

[ Molecular Weight ]:
229.114

[ Flash Point ]:
114.1±23.8 °C

[ Exact Mass ]:
228.014969

[ PSA ]:
9.23000

[ LogP ]:
3.72

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.532

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S37/39-S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2909309090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2909309090

[ Summary ]:
2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Sequential one-pot ruthenium-catalyzed azide-alkyne cycloaddition from primary alkyl halides and sodium azide.

J. Org. Chem. 76(7) , 2355-9, (2011)

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 re...

Titanocene-catalyzed regioselective alkylation of styrenes with grignard reagents using beta-bromoethyl ethers, thioethers, or amines.

Chem. Asian J. 3(8-9) , 1472-1478, (2008)

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 cata...

Electrochemical reduction of 1, 4-dihalobutanes at carbon cathodes in dimethylformamide. Pritts WA and Peters DG.

J. Electroanal. Chem. 380(1) , 147-160, (1995)