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Factory Supply Industrial Grade 6-Chlorohexanol 2009-83-8 with Best Price
- 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
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Preparation |
6-Chlorohexanol is obtained from the reaction of 1,6-Hexanediol with hydrochloric acid. |
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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
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chlorure de trimethylammonio-6 hexanol-1
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821-41-0
5-Hexen-1-ol
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2009-83-8
6-chloro-1-hexanol
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1862-07-3
6-(N,N-dimethylamino)-1-hexanol
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58390-19-5
6-(dimethylamino)-1-methoxyhexane
| Conditions | Yield |
|---|---|
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at 220 ℃;
Product distribution;
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928-89-2
6-chlorohexene
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2009-83-8
6-chloro-1-hexanol
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111-27-3
hexan-1-ol
| Conditions | Yield |
|---|---|
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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;
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2009-83-8 Upstream products
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629-11-8
1,6-hexanediol
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4224-62-8
6-chlorohexanoic acid
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592-90-5
oxepane
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928-89-2
6-chlorohexene
2009-83-8 Downstream products
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149265-11-2
N-(6-hydroxyhexyl)-N'-phenylpiperazine
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17976-80-6
7-hydroxyheptanenitrile
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98433-41-1
6-(methylthio)hexan-1-ol
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6294-17-3
1-bromo-6-chlorohexane
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