6294-17-3

  • Product Name:1-Bromo-6-Chlorohexane
  • Molecular Formula:C6H12BrCl
  • Purity:99%
  • Molecular Weight:199.518
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Product Details;

CasNo: 6294-17-3

Molecular Formula: C6H12BrCl

Manufacturer supply 1-Bromo-6-Chlorohexane 6294-17-3 with sufficient stock and high standard

  • Molecular Formula:C6H12BrCl
  • Molecular Weight:199.518
  • Vapor Pressure:0.196mmHg at 25°C 
  • Refractive Index:n20/D 1.481(lit.)  
  • Boiling Point:217.4 °C at 760 mmHg 
  • Flash Point:101.1 °C 
  • PSA:0.00000 
  • Density:1.311 g/cm3 
  • LogP:3.18050 

1-Bromo-6-chlorohexane(Cas 6294-17-3) Usage

InChI:InChI=1/C6H12BrCl/c7-5-3-1-2-4-6-8/h1-6H2

6294-17-3 Relevant articles

A novel stereoselective one-pot conversion of alcohols into alkyl halides mediated by N,N′-diisopropylcarbodiimide

Crosignani, Stefano,Nadal, Brice,Li, Zhengning,Linclau, Bruno

, p. 260 - 261 (2007/10/03)

Alcohols can be converted in high yields...

Process for the preparation of α-bromo, ω-chloroalkanes

-

, (2008/06/13)

Described is a process for easily prepar...

Imine-Directed Metalation of o-Tolualdehyde: The Use of Catalytic Amine Base. A Route to 2-(8-Phenyloctyl)benzaldehyde

Forth, Michael A.,Mitchell, Michael B.,Smith, Stephen A. C.,Gombatz, Kerry,Snyder, Lawrence

, p. 2616 - 2619 (2007/10/02)

-

A New and Efficient One-Pot Preparation of Alkyl Halides From Alcohols

Camps, Francisco,Gasol, Vicens,Guerrero, Angel

, p. 511 - 512 (2007/10/02)

Primary alkanols and 2-alkenols are conv...

6294-17-3 Process route

1,6-hexanediol
629-11-8

1,6-hexanediol

1-bromo-6-chlorohexane
6294-17-3

1-bromo-6-chlorohexane

6-chloro-1-hexanol
2009-83-8

6-chloro-1-hexanol

Conditions
Conditions Yield
With hydrogenchloride; sodium hydroxide; zinc(II) chloride;
34%
6-chloro-1-hexanol
2009-83-8

6-chloro-1-hexanol

1-bromo-6-chlorohexane
6294-17-3

1-bromo-6-chlorohexane

Conditions
Conditions Yield
6-chloro-1-hexanol; With diisopropyl-carbodiimide; copper(II) bis(trifluoromethanesulfonate); In tetrahydrofuran; at 100 ℃; for 0.0833333h; microwave irradiation;
With Acetyl bromide; In tetrahydrofuran; at 150 ℃; for 0.0833333h; Further stages.; microwave irradiation;
96%
With phosphorus tribromide;
 
 
 
Multi-step reaction with 2 steps
1: tetrahydrofuran / 0.25 h / Ambient temperature
2: LiBr / tetrahydrofuran; hexamethylphosphoric acid triamide / 3 h / Heating
With lithium bromide; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide;
 
 
 

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