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2-ACETYLCYCLOHEXANONE

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2-ACETYLCYCLOHEXANONE Basic information

Product Name:
2-ACETYLCYCLOHEXANONE
Synonyms:
  • alpha-Acetylcyclohexanone
  • 2-acetylcyclohexan-1-one
  • 2-Acetylcyclohexanone,98%
  • 2-Acetylcyclohexanone,97%
  • 2-ACETYLCYCLOHEXANONE FOR SYNTHESIS
  • 2-Acetyl-1-cyclohexanone
  • 2-acetyl-cyclohexanon
  • Acetylcyclohexanone
CAS:
874-23-7
MF:
C8H12O2
MW:
140.18
EINECS:
212-858-5
Product Categories:
  • C7 to C8
  • Carbonyl Compounds
  • Ketones
Mol File:
874-23-7.mol
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2-ACETYLCYCLOHEXANONE Chemical Properties

Melting point:
-11°C
Boiling point:
111-112 °C/18 mmHg (lit.)
Density 
1.078 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.509(lit.)
Flash point:
175 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Chloroform, Ethyl Acetate
form 
Liquid
pka
10.91±0.20(Predicted)
color 
Clear colorless to light yellow
Water Solubility 
Not miscible in water.
BRN 
1858621
InChIKey
OEKATORRSPXJHE-UHFFFAOYSA-N
CAS DataBase Reference
874-23-7(CAS DataBase Reference)
EPA Substance Registry System
Cyclohexanone, 2-acetyl- (874-23-7)
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Safety Information

Safety Statements 
23-24/25
WGK Germany 
3
TSCA 
Yes
HS Code 
29142990

MSDS

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2-ACETYLCYCLOHEXANONE Usage And Synthesis

Chemical Properties

clear colorless to light yellow liquid

Uses

2-Acetylcyclohexanone was used in the synthesis of anilinoethanolamines.

Uses

2-Acetylcyclohexanone is used in the synthesis of 1-(pyridyl)ethanol derivatives that can reduce keto-esters and ketones. Also used in the synthesis of phenothiazine derivatives that can inhibit prote in farnesyltransferase molecules and some that show anti-proliferative activity.

General Description

The keto-enol tautomerism of 2-acetylcyclohexanone (ACHE) in water was studied.

Purification Methods

Dissolve it in ligroin (b 30-60o), wash it with saturated aqueous NaHCO3, dry over Drierite and fractionate in a vacuum. [Perfetti & Levine J Am Chem Soc 75 626 1953, Manyik et al. J Am Chem Soc 75 5030 1953, Eistert & Reiss Chem Ber 87 108 1954.] It forms a Cu salt which crystallises in green leaflets from EtOH, m 162-163o [UV: McEntee & Pinder J Chem Soc 4419 1957].

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