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(1-Bromoethyl)benzene / 25 G

Purity: 97 %
Synonym: α-Methylbenzyl bromide; 1-Phenylethyl bromide; 1-Bromo-1-phenylethane
Molecular Formula: C6H5CH(CH3)Br
Molecular Weight: 185.06
SKU: MND-50059
CAS Number: 585-71-7
MDL number: MFCD00000139
EC Number: 209-560-2
PubChem: 24854291
Form: liquid
Packing size: 25 G  
31.22 EUR



Safety Information


Hazard Statements

H315
H319
H335

Precautionary Statements

P280
P264
P305 + P351 + P338
P261
P271
P302 + P352

Pictograms



Properties

Signal WordWarning
Flash Point (C)82 °C - closed cup
Flash Point (F)179.6 °F - closed cup
Density1.356 g/mL at 25 °C (lit.)
Boiling Point94 °C/16 mmHg (lit.)

 Product Description

(1-Bromoethyl)benzene is a chemical compound commonly used as a versatile building block in organic synthesis. Its primary application lies in its role as a key intermediate for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals.

 

Application:

Utilized as a versatile building block, (1-Bromoethyl)benzene serves as a crucial intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, contributing to diverse chemical processes.

 

 

Articles:

- Synthesis of 4,6-diarylpyrimidin-2(1H)-one derivatives from benzyl halides and (1-bromoethyl)benzene under solvent-free conditions

Publication Date: 16 Jul 2018

Mallappa Beerappa & Kalegowda Shivashankar

https://doi.org/10.1080/00397911.2018.1479757

 

- Controlled radical polymerization catalyzed by copper(I)–sparteine complexes

Publication Date: 21 January 2000

Bin Yu, Eli Ruckenstein

https://doi.org/10.1002/(SICI)1099-0518(19991115)37:22<4191::AID-POLA19>3.0.CO;2-V

 

- Mechanism of formation of mercapturic acids from (1-bromoethyl)benzene and (2-bromoethyl)benzene in the rat

Publication Date: 30 Sep 2009

F. Seutter-berlage, L. P. C. Delbressine, F. L. M. Smeets & M. A. P. Wagenaars-zegers

https://doi.org/10.3109/00498257909038734