CAS 874-23-7|2-Acetylcyclohexanone

Introduction:Basic information about CAS 874-23-7|2-Acetylcyclohexanone, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name2-Acetylcyclohexanone
CAS Number874-23-7Molecular Weight140.180
Density1.0±0.1 g/cm3Boiling Point224.3±0.0 °C at 760 mmHg
Molecular FormulaC8H12O2Melting Point/
MSDSUSAFlash Point79.4±0.0 °C

Names

Name2-Acetylcyclohexanone
SynonymMore Synonyms

Chemical & Physical Properties

Density1.0±0.1 g/cm3
Boiling Point224.3±0.0 °C at 760 mmHg
Molecular FormulaC8H12O2
Molecular Weight140.180
Flash Point79.4±0.0 °C
Exact Mass140.083725
PSA34.14000
LogP0.08
Vapour Pressure0.1±0.4 mmHg at 25°C
Index of Refraction1.464
InChIKeyOEKATORRSPXJHE-UHFFFAOYSA-N
SMILESCC(=O)C1CCCCC1=O

Safety Information

Personal Protective EquipmentEyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US)
Safety PhrasesS23-S24/25
RIDADRNONH for all modes of transport
WGK Germany3
HS Code2914299000

Customs

HS Code2914299000
Summary2914299000. other cyclanic, cyclenic or cyclotherpenic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles4

More Articles
Tautomerization of 2-acetylcyclohexanone. 1. Characterization of keto-enol/enolate equilibria and reaction rates in water.

J. Org. Chem. 68(7) , 2680-8, (2003)

The keto-enol tautomerism of 2-acetylcyclohexanone (ACHE) was studied in water under different experimental conditions. By contrast with other previously studied beta-diketones, the keto-enol intercon...

Copper-catalyzed amination of (bromophenyl)ethanolamine for a concise synthesis of aniline-containing analogues of NMDA NR2B antagonist ifenprodil.

Org. Biomol. Chem. 8(5) , 1111-20, (2010)

An operationally simple and concise synthesis of anilinoethanolamines, as NMDA NR2B receptor antagonist ifenprodil analogues, was developed via a copper-catalyzed amination of the corresponding bromoa...

An alternative to the classical α-arylation: the transfer of an intact 2-iodoaryl from ArI(O₂CCF₃)₂.

Angew. Chem. Int. Ed. Engl. 53(42) , 11298-301, (2014)

The α-arylation of carbonyl compounds is generally accomplished under basic conditions, both under metal catalysis and via aryl transfer from the diaryl λ(3)-iodanes. Here, we describe an alternative ...

Synonyms

2-Acetylcyclohexanone
2-acetylcyclohexanone for synthesis
2-Acetyl-1-cyclohexanone
2-acetylcyclohexa
2-acetyl cyclohexanone
Cyclohexanone, 2-acetyl-
MFCD00001633
EINECS 212-858-5
cyclohexanone,2-acetyl-
2-acetylcyclohexanon
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