2-Benzoylcyclohexanone

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Names

[ CAS No. ]:
3580-38-9

[ Name ]:
2-Benzoylcyclohexanone

[Synonym ]:
2-Benzoylcyclohexanone
Cyclohexanone,2-benzoyl
MFCD00524769
2-Benzoylcycloheanone
benzoylcyclohexanone
2-Benzoyl-cyclohexanon

Chemical & Physical Properties

[ Density]:
1.123 g/cm3

[ Boiling Point ]:
343.7ºC at 760 mmHg

[ Melting Point ]:
88-91ºC(lit.)

[ Molecular Formula ]:
C13H14O2

[ Molecular Weight ]:
202.24900

[ Flash Point ]:
128.9ºC

[ Exact Mass ]:
202.09900

[ PSA ]:
34.14000

[ LogP ]:
2.62860

[ Index of Refraction ]:
1.551

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2914399090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Cyclohexanone
  • Benzoyl chloride
  • Methyl benzoate
  • Sodium tert-pentoxide
  • 1-Methoxy-2-propanol
  • cyclohexenone
  • Benzoyl cyanide
  • 1-(trimethylsilyloxy)-cyclohex-1-ene
  • Benzoyl Fluoride
  • PHENYL DIAZOMETHYL KETONE

DownStream

  • Ethyl benzoate
  • Methyl benzoate
  • methyl 7-phenyl-7-oxo-heptanoate
  • Cyclohexanone
  • 1-phenylcyclohex-1-ene
  • benzoic acid,cyclohexen-1-ol
  • benzene
  • fema 2860

Customs

[ HS Code ]: 2914399090

[ Summary ]:
2914399090. other aromatic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

Configurational stability of 2-benzoylcyclohexanone: unexpected solvent effects on the rate of racemization.

Chirality 17(4) , 171-6, (2005)

The kinetics of the racemization of 2-benzoylcyclohexanone 1 in hexanes, ethanol, and mixtures thereof have been investigated by time dependence of enantiomeric purity using enantioselective HPLC. In ...

The regioselective preparation of 1, 3-diketones within a micro reactor. Wiles C, et al.

Chem. Commun. (Camb.) 10 , 1034-1035, (2002)


More Articles

Related Compounds

  • 4-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4,4,4-trifluorobutanamido]butanoic acid
  • (2S)-2-{2-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)piperidin-1-yl]acetamido}-3-methylbutanoic acid
  • 4-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methylbutanamido]-3-fluorobenzoic acid
  • 2-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)oxolane-3-amido]benzoic acid
  • 2-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-N-methylpropanamido]-2-methylpropanoic acid
  • 4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-[(1-methanesulfonyl-2-methylpropan-2-yl)carbamoyl]butanoic acid
  • (2R)-2-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylpentanamido]-4-hydroxybutanoic acid
  • 1-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylpentanoyl]azetidine-2-carboxylic acid
  • 2-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylpentanamido]pent-4-ynoic acid
  • 5-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylpentanamido]-4-methylpentanoic acid
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