Benzyl 2-Bromoethyl Ether

Names

[ Name ]:
Benzyl 2-Bromoethyl Ether

[Synonym ]:
Benzene, ((2-bromoethoxy)methyl)-
(2-Bromoethoxymethyl)benzene
[(2-Bromoethoxy)methyl]benzene
MFCD01321307
Benzene, [(2-bromoethoxy)methyl]-
Benzyl 2-Bromoethyl Ether
((2-Bromoethoxy)methyl)benzene
2-bromoethoxymethylbenzene
Ether, benzyl 2-bromoethyl
Benzyloxyethyl Bromide
2-benzyloxy-1-bromoethane

Biological Activity

[Description]:

Benzyl 2-bromoethyl ether is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
1.36

[ Boiling Point ]:
254 ºC

[ Molecular Formula ]:
C₉H₁₁BrO

[ Molecular Weight ]:
215.09

[ Flash Point ]:
113 ºC

[ Exact Mass ]:
213.999313

[ PSA ]:
9.23000

[ LogP ]:
3.00

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

[ Index of Refraction ]:
1.543

[ Water Solubility ]:
Slightly soluble in water

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xn: Harmful;

[ Risk Phrases ]:
R22

[ Safety Phrases ]:
24/25

[ RIDADR ]:
UN 3334

[ 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

Total synthesis and conformational analysis of the antifungal agent (-)-PF1163B.

Org. Lett. 5 , 4049-4052, (2003)

[reaction: see text]. (-)-PF1163B, a new macrocyclic antifungal antibiotic isolated from Streptomyces sp., has been prepared in eight steps from (S)-citronellene. The key step is a ring-closing metath...

Chem. Mater. 17 , 1618, (2005)

680290

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