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6-Chlorohexanol

  • CAS No.: 2009-83-8
  • Purity: 99%
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  • Molecular Formula: C6H13ClO
  • Molecular Weight: 136.622
  • Appearance/Colour: clear colorless to pale yellow liquid 
  • Vapor Pressure: 0.0378mmHg at 25°C 
  • Melting Point: 129-130ºC 
  • Refractive Index: n20/D 1.456(lit.)  
  • Boiling Point: 212.8 °C at 760 mmHg 
  • PKA: 15.17±0.10(Predicted) 
  • Flash Point: 98.9 °C 
  • PSA: 20.23000 
  • Density: 1.001 g/cm3 
  • LogP: 1.77790 

6-Chlorohexanol(Cas 2009-83-8) Usage

Preparation

6-Chlorohexanol is obtained from the reaction of 1,6-Hexanediol with hydrochloric acid.

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 3, p. 446, 1955Tetrahedron Letters, 36, p. 3161, 1995 DOI: 10.1016/0040-4039(95)00501-3

InChI:InChI=1/C6H13ClO/c7-5-3-1-2-4-6-8/h8H,1-6H2

2009-83-8 Relevant articles

Chemoselective Cleavage of Si-C(sp3) Bonds in Unactivated Tetraalkylsilanes Using Iodine Tris(trifluoroacetate)

Matsuoka, Keitaro,Komami, Narumi,Kojima, Masahiro,Mita, Tsuyoshi,Suzuki, Kimichi,Maeda, Satoshi,Yoshino, Tatsuhiko,Matsunaga, Shigeki

, p. 103 - 108 (2021/01/13)

Organosilanes are synthetically useful r...

Method for synthesizing 6-chloro-1-hexanol by taking 1,6-hexanediol and cyanuric chloride as raw materials

-

Paragraph 0035-0062, (2021/01/29)

The invention relates to the field of or...

A highly active and air-stable ruthenium complex for the ambient temperature anti-markovnikov reductive hydration of terminal alkynes

Zeng, Mingshuo,Li, Le,Herzon, Seth B.

supporting information, p. 7058 - 7067 (2014/06/09)

The conversion of terminal alkynes to fu...

Temporal separation of catalytic activities allows anti-Markovnikov reductive functionalization of terminal alkynes

Li, Le,Herzon, Seth B.

, p. 22 - 27 (2014/01/17)

There is currently great interest in the...

2009-83-8 Process route

chlorure de trimethylammonio-6 hexanol-1

chlorure de trimethylammonio-6 hexanol-1

5-Hexen-1-ol
821-41-0

5-Hexen-1-ol

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

6-chloro-1-hexanol

6-(N,N-dimethylamino)-1-hexanol
1862-07-3

6-(N,N-dimethylamino)-1-hexanol

6-(dimethylamino)-1-methoxyhexane
58390-19-5

6-(dimethylamino)-1-methoxyhexane

Conditions
Conditions Yield
at 220 ℃; Product distribution;
6-chlorohexene
928-89-2

6-chlorohexene

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

6-chloro-1-hexanol

hexan-1-ol
111-27-3

hexan-1-ol

Conditions
Conditions Yield
With sodium hydroxide; sodium tetrahydroborate; dihydrogen peroxide; sodium iodide; Yield given. Multistep reaction. Yields of byproduct given; 1.) diglyme, 25 deg C, electrolysis, 2.) 25 deg C, 2 h;

2009-83-8 Upstream products

  • 629-11-8
    629-11-8

    1,6-hexanediol

  • 4224-62-8
    4224-62-8

    6-chlorohexanoic acid

  • 592-90-5
    592-90-5

    oxepane

  • 928-89-2
    928-89-2

    6-chlorohexene

2009-83-8 Downstream products

  • 149265-11-2
    149265-11-2

    N-(6-hydroxyhexyl)-N'-phenylpiperazine

  • 17976-80-6
    17976-80-6

    7-hydroxyheptanenitrile

  • 98433-41-1
    98433-41-1

    6-(methylthio)hexan-1-ol

  • 6294-17-3
    6294-17-3

    1-bromo-6-chlorohexane

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