2-Acetylcyclohexanone structure
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Common Name | 2-Acetylcyclohexanone | ||
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CAS Number | 874-23-7 | Molecular Weight | 140.180 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 224.3±0.0 °C at 760 mmHg | |
Molecular Formula | C8H12O2 | Melting Point | N/A | |
MSDS | USA | Flash Point | 79.4±0.0 °C |
Name | 2-Acetylcyclohexanone |
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Synonym | More Synonyms |
Density | 1.0±0.1 g/cm3 |
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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 |
Personal Protective Equipment | Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US) |
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Safety Phrases | S23-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2914299000 |
Precursor 8 | |
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DownStream 8 | |
HS Code | 2914299000 |
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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% |
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... |
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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... |
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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 ... |
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 |