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Cycloheptanone information


Cycloheptanone
Names
Preferred IUPAC name
Cycloheptanone
Other names
Suberone
Identifiers
CAS Number
  • 502-42-1 checkY
3D model (JSmol)
  • Interactive image
ChEMBL
  • ChEMBL18607 checkY
ChemSpider
  • 9971 checkY
ECHA InfoCard 100.007.216 Edit this at Wikidata
EC Number
  • 207-937-6
PubChem CID
  • 10400
UNII
  • QH80295937 checkY
CompTox Dashboard (EPA)
  • DTXSID8060113 Edit this at Wikidata
InChI
  • InChI=1S/C7H12O/c8-7-5-3-1-2-4-6-7/h1-6H2 checkY
    Key: CGZZMOTZOONQIA-UHFFFAOYSA-N checkY
SMILES
  • O=C1CCCCCC1
Properties
Chemical formula
 C7H12O
Molar mass 112.172 g·mol−1
Appearance Colorless liquid
Density 0.949 g/cm3 (20 °C)[1]
Boiling point 179 to 181 °C (354 to 358 °F; 452 to 454 K)[1]
Solubility in water
 Insoluble
Hazards
GHS labelling:
Pictograms
 GHS02: FlammableGHS05: CorrosiveGHS07: Exclamation mark
Signal word
 Danger
Hazard statements
 H226, H302, H318
Precautionary statements
 P210, P233, P240, P241, P242, P243, P264, P270, P280, P301+P312, P303+P361+P353, P305+P351+P338, P310, P330, P370+P378, P403+P235, P501
Flash point 56 °C (133 °F; 329 K)[2]
Related compounds
Related cyclic ketones
 Cyclohexanone, Cyclooctanone, Tropinone
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

Cycloheptanone, (CH2)6CO, is a cyclic ketone also referred to as suberone. It is a colourless volatile liquid. Cycloheptanone is used as a precursor for the synthesis of pharmaceuticals.

  1. ^ a b The Merck Index, 11th Edition, 2728
  2. ^ Cycloheptanone at Sigma-Aldrich

and 15 Related for: Cycloheptanone information

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Cycloheptanone

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Cycloheptanone, (CH2)6CO, is a cyclic ketone also referred to as suberone. It is a colourless volatile liquid. Cycloheptanone is used as a precursor for...

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Tropinone

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Richard Willstätter in 1901. It started from the seemingly related cycloheptanone, but required many steps to introduce the nitrogen bridge; the overall...

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Caprolactam

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Caprolactam Names Preferred IUPAC name Azepan-2-one Other names 1-Aza-2-cycloheptanone 2-Azacycloheptanone ε-Caprolactam Capron PK4 Cyclohexanone iso-oxime...

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Bisulfite

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reported to allow differentiation between the primary reaction product cycloheptanone and the main contaminant cyclooctanone. Another use of bisulfite in...

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C7H12O

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The molecular formula C7H12O (molar mass 112.17 g/mol) may refer to: Cycloheptanone Methylcyclohexanone Norborneols endo-Norborneol exo-Norborneol This...

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Cycloheptane

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pharmaceutical drugs. It may be derived by Clemmensen reduction from cycloheptanone. Cycloheptane vapour is irritating to the eyes and may cause respiratory...

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Nitromethane

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D. L.; Anderson, A. G. Jr.; de Boer, T. J.; Backer, H. J. (1963). "Cycloheptanone". Organic Syntheses; Collected Volumes, vol. 4, p. 221. Noland, W. E...

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Reduction of nitro compounds

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H. J.; Wade, R. H.; Pearson, D. L.; Anderson, Jr., A. G. (1963). "Cycloheptanone". Organic Syntheses{{cite journal}}: CS1 maint: multiple names: authors...

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Heptanone

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(Ethyl sec-butyl ketone) 5-Methyl-3-hexanone (Ethyl isobutyl ketone) Cycloheptanone Methylcyclohexanone 2-Methylcyclohexanone 3-Methylcyclohexanone 4-Methylcyclohexanone...

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Cyclohexanone

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(Immediate danger) 700 ppm Related compounds Related ketones Cyclopentanone, cycloheptanone Related compounds Cyclohexanol Except where otherwise noted, data are...

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Pimelic acid

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pimelic acid. Pimelic acid is produced commercially by oxidation of cycloheptanone with dinitrogen tetroxide. Other routes include the relatively unselective...

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Cycloheptatriene

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synthesis of Richard Willstätter in 1901. This synthesis started from cycloheptanone and established the seven membered ring structure of the compound. Cycloheptatriene...

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List of compounds with carbon number 7

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C7H12N2O2 ectylurea 95-04-5 C7H12O allyl methallyl ether 14289-96-4 C7H12O cycloheptanone 502-42-1 C7H12O cyclohexanecarboxaldehyde 2043-61-0 C7H12O dicyclopropyl...

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Tropone

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moment for tropone is 4.17 D compared to a value of only 3.04 D for cycloheptanone. This difference is consistent with stabilization of the dipolar resonance...

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Ciclafrine

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ethers. Ciclafrine can be prepared by the reaction of norfenefrine with cycloheptanone. Ganellin CR, Triggle DJ (21 November 1996). Dictionary of Pharmacological...

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