<Suppliers Price>

2-Acetylcyclohexanone

Names

[ CAS No. ]:
874-23-7

[ Name ]:
2-Acetylcyclohexanone

[Synonym ]:
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

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
224.3±0.0 °C at 760 mmHg

[ Molecular Formula ]:
C8H12O2

[ Molecular Weight ]:
140.180

[ Flash Point ]:
79.4±0.0 °C

[ Exact Mass ]:
140.083725

[ PSA ]:
34.14000

[ LogP ]:
0.08

[ Vapour Pressure ]:
0.1±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.464

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US)

[ Safety Phrases ]:
S23-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2914299000

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2914299000

[ Summary ]:
2914299000. 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%

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 ...


More Articles


Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.