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Quality Factory Hot Selling 2-CHLOROPHENETHYL BROMIDE 16793-91-2 with Fast Shipping

  • Molecular Formula: C8H8 Br Cl
  • Molecular Weight: 219.509
  • Vapor Pressure: 0.0623mmHg at 25°C 
  • Refractive Index: n20/D 1.5707(lit.)  
  • Boiling Point: 110-112 °C10 mm Hg  
  • Flash Point: >230 °F  
  • PSA: 0.00000 
  • Density: 1.4569 g/mL at 25 °C(lit.)  
  • LogP: 3.27740 

2-CHLOROPHENETHYL BROMIDE(Cas 16793-91-2) Usage

General Description

2-Chlorophenethyl bromide is an organic compound that consists of a benzene ring with a chlorine atom and a bromine atom attached to it. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. This chemical is also known for its application as a reagent in organic chemistry, particularly in the preparation of various types of compounds including ethers and esters. It is a colorless to pale yellow liquid that is volatile and has a strong, unpleasant odor. 2-Chlorophenethyl bromide is also known by its alternative name, 2-bromoethyl benzene, and has the chemical formula C8H8BrCl. It is important to handle this compound with caution as it is considered to be toxic and may cause irritation to the skin, eyes, and respiratory system.

InChI:InChI=1/C8H8BrCl/c9-6-5-7-3-1-2-4-8(7)10/h1-4H,5-6H2

16793-91-2 Relevant articles

-

Barnes,Konort

, p. 303 (1953)

-

Para-Selective C-H Borylation of Common Arene Building Blocks Enabled by Ion-Pairing with a Bulky Countercation

Mihai, Madalina T.,Williams, Benjamin D.,Phipps, Robert J.

supporting information, p. 15477 - 15482 (2019/10/11)

The selective functionalization of C-H b...

Preparation method for hemihydrate lorcaserin hydrochloride

-

Paragraph 0106; 0107, (2017/08/28)

The invention discloses a preparation me...

Scalable anti-Markovnikov hydrobromination of aliphatic and aromatic olefins

Galli, Marzia,Fletcher, Catherine J.,Del Pozo, Marc,Goldup, Stephen M.

supporting information, p. 5622 - 5626 (2016/07/06)

To improve access to a key synthetic int...

Construction of chiral 2-substituted octahydroindoles from cyclic ketones and nitroolefins bearing only one α-substituent

Han, Yong,Zheng, Bo,Peng, Yungui

supporting information, p. 1136 - 1142 (2015/04/22)

A dual catalytic system has been develop...

16793-91-2 Process route

2-(2-chlorophenyl)-1-ethanol
19819-95-5

2-(2-chlorophenyl)-1-ethanol

1-(2-bromoethyl)-2-chlorobenzene
16793-91-2

1-(2-bromoethyl)-2-chlorobenzene

Conditions
Conditions Yield
With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 0 - 20 ℃;
84%
With phosphorus tribromide; In benzene; 1.) 0 deg C, 1 h, 2.) reflux, 3 h;
78%
With phosphorus tribromide;
With carbon tetrabromide; triphenylphosphine; In dichloromethane;
With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 0 - 25 ℃;
With phosphorus tribromide; at 0 - 80 ℃; for 2.16667h;
22.4 g
2-chlorostyrene
2039-87-4,107830-52-4,26125-41-7

2-chlorostyrene

1-(2-bromoethyl)-2-chlorobenzene
16793-91-2

1-(2-bromoethyl)-2-chlorobenzene

Conditions
Conditions Yield
With hydrogen bromide; acetic acid; In hexane; at 0 ℃; for 2h;
99%

16793-91-2 Upstream products

  • 19819-95-5
    19819-95-5

    2-(2-chlorophenyl)-1-ethanol

  • 2444-36-2
    2444-36-2

    2'-chloro-benzeneacetic acid

  • 2039-87-4
    2039-87-4

    2-chlorostyrene

16793-91-2 Downstream products

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    1-[2-(2-Chloro-phenyl)-ethyl]-4-(3-methoxy-phenyl)-3,3,4-trimethyl-piperidine

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    S-(2-(2-chlorophenyl)ethyl)isothiourea hydrobromide

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    1643-28-3

    3-(2-chlorophenyl)propanoic acid

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