Cyclopentane, methylene-

• Formula: C₆H₁₀
• Molecular weight: 82.1436
• IUPAC Standard InChI: InChI=1S/C6H10/c1-6-4-2-3-5-6/h1-5H2 Copy

  
• IUPAC Standard InChIKey: NFJPEKRRHIYYES-UHFFFAOYSA-N Copy
• CAS Registry Number: 1528-30-9
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: Methylenecyclopentane; 1-Methylenecyclopentane
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
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Normal boiling point

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]

Pinchas, Shabtai, et al., 1959
Pinchas, S.; Shabtai, J.; Herling, J.; Gil-Av, E., The Preparation and Infrared Spectra of the Three Ethylcyclopentenes, Methylene-, and ethylidenecyclopentane, J. Inst. Pet., 1959, 45, 311. [all data]

Searles, Nickerson, et al., 1959
Searles, S.; Nickerson, R.G.; Witsiepe, W.K., Oxetanes. IX. Structural and Solvent Effects in the Reaction of γ-Bromo Alcohols with Base, J. Org. Chem., 1959, 24, 1839. [all data]

Turner and Garner, 1958
Turner, R.B.; Garner, R.H., Heats of Hydrogenation V. Relative Stabilities in Certain Exocyclic- Endocyclic Olefin Pairs, J. Am. Chem. Soc., 1958, 80, 1424. [all data]

Cope, Bumgardner, et al., 1957
Cope, A.C.; Bumgardner, C.L.; Schweizer, E.E., Amine Oxides IV. Alicyclic Olefins from Aine Oxides and Quaternary Ammonium Hydroxides, J. Am. Chem. Soc., 1957, 79, 4729-33. [all data]

Schubert and Leahy, 1957
Schubert, W.M.; Leahy, S.M., J. Am. Chem. Soc., 1957, 79, 381-5. [all data]

Chiurdoglu, Laune, et al., 1956
Chiurdoglu, G.; Laune, J.; Poelmans, M., Acyclic compounds with Quarternary Carbon IV. Conjugation with 1-Ethoxycaronylcycloprpanesprirocyclanes, Bull Soc. Chim. Belges, 1956, 65, 257-69. [all data]

Traynham and Pascual, 1956
Traynham, J.G.; Pascual, O.S., J. Org. Chem., 1956, 21, 1362. [all data]

Slobodin and Blinova, 1953
Slobodin, Ya.M.; Blinova, M.V., Spirohexane, Zh. Obshch. Khim., 1953, 23, 1994-7. [all data]

Sorm and Beranek, 1953
Sorm, F.; Beranek, J., Synthesis of methylenecycloalkanes, Chem. Listy, 1953, 47, 708. [all data]

Van derbij and Kooijman, 1952
Van derbij, J.R.; Kooijman, E.C., Properties of a number of cyclic olefins, Recl. Trav. Chim. Pays-Bas, 1952, 71, 837. [all data]

Cook, 1949
Cook, N.C., Penn. State Univ., 1949. [all data]

Vogel, 1938
Vogel, A.I., J. Chem. Soc., 1938, 1938, 1323. [all data]

Wallach, 1906
Wallach, O., Justus Liebigs Ann. Chem., 1906, 347, 316-46. [all data]

Notes

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• Symbols used in this document:
  

  Tboil

  Boiling point

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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