Cyclopentene

• Formula: C₅H₈
• Molecular weight: 68.1170
• IUPAC Standard InChI: InChI=1S/C5H8/c1-2-4-5-3-1/h1-2H,3-5H2 Copy

  
• IUPAC Standard InChIKey: LPIQUOYDBNQMRZ-UHFFFAOYSA-N Copy
• CAS Registry Number: 142-29-0
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
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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

Go To: Top, Normal boiling point, Notes

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]

Samartsev and Ogloblin, 1965
Samartsev, M.A.; Ogloblin, K.A., Interaction of nitrosyl Chloride with unsaturate compounds. XVII. cis-trans -isomerism of aliphatic chloronitroso compounds, J. Org. Chem. USSR (Engl. Transl.), 1965, 1, 29-34. [all data]

Anonymous, 1959
Anonymous, R., , Am. Pet. Inst. Res. Proj. 6, Carnegie-Mellon Univ., 1959. [all data]

Mark and Pines, 1956
Mark, V.; Pines, H., Carbanion and Thermal Reactions of Some Simple Olefins, J. Am. Chem. Soc., 1956, 78, 5946-50. [all data]

Plate and Stanko, 1956
Plate, A.F.; Stanko, V.I., Preparation of Cyclopentene from Cyclopentadiene, Izvest. Akad. Nauk S.S.S.R., 1956, 1956, 1148-50. [all data]

Traynham and Sehnert, 1956
Traynham, J.G.; Sehnert, M.F., Ring Size and Reactivity of Cyclic Olefins: Complexation with Aqueous Silver Ion, J. Am. Chem. Soc., 1956, 78, 4024. [all data]

Timmermans and Hennaut-Roland, 1955
Timmermans, J.; Hennaut-Roland, M., Work of the International Bureau of Physical-Chemical Standards. IX. The Physical Constants of Twenty Organic Compounds, J. Chim. Phys. Phys.-Chim. Biol., 1955, 52, 223. [all data]

Conn and Schneider, 1954
Conn, W.K.; Schneider, A., Formation of Hydronaphthalenes from Cyclopoentyl Rings in Acid-catalyzed Reactions, J. Am. Chem. Soc., 1954, 76, 4578. [all data]

Bollinger, Hayes, et al., 1953
Bollinger, F.W.; Hayes, F.N.; Siegel, S., The Base-Catalyzed Decomposition of N-Nitroso-N-cyclopentylurethan, J. Am. Chem. Soc., 1953, 75, 1729-30. [all data]

Stoll, Lindenmann, et al., 1953
Stoll, A.; Lindenmann, A.; Jucker, E., Alkaloid Syntheses II. The Synthesis of Glutaraldehyde, Helv. Chim. Acta, 1953, 36, 268-74. [all data]

Adkins and Watkins, 1951
Adkins, H.; Watkins, S.H., Investigation of the Properties of Alumina ex-Aliminum Isopropxide as a Catalyst for Dehydrations., J. Am. Chem. Soc., 1951, 73, 2184. [all data]

Roberts and Chambers, 1951
Roberts, J.D.; Chambers, V.C., Small ring compd. VIII. some nucleophilic displacement reaction of cyclo- propyl, cyclobutyl, cyclopentyl & cyclohexyl p-toluenesulfonates & halides, J. Am. Chem. Soc., 1951, 73, 5034. [all data]

Kazanskii, Terent'eva, et al., 1950
Kazanskii, B.A.; Terent'eva, E.M.; Bulanova, T.F., Synthesis of Organic Compounds: Cyclopentane fro Cyclopentanone, Akad. Nauk S.S.S.R., Inst. Org. Khim. Sintegy Org. Sodinenil Sbornik, 1950, I, 161-4. [all data]

Foehr and Fenske, 1949
Foehr, E.G.; Fenske, M.R., Magneto-optic Rotation of Hydrocarbons, Ind. Eng. Chem., 1949, 41, 1956. [all data]

Forziati and Rossini, 1948
Forziati, A.F.; Rossini, F.D., Personal Commun., 1948. [all data]

Robey and Wiese, 1948
Robey, R.F.; Wiese, H.K., Chemical Analysis of Refinery C5 Hydrocarbon Fractions, Anal. Chem., 1948, 20, 926-33. [all data]

Gerding and van der Vet, 1946
Gerding, H.; van der Vet, A.P., Raman spectra of the seven isomeric pentenes and quantitative analysis of two mixtures by means of the Raman effect, Recl. Trav. Chim. Pays-Bas, 1946, 64, 257. [all data]

Mousseron, 1946
Mousseron, M., Bull. Soc. Chim. Fr., 1946, 1946, 218. [all data]

Anonymous, 1943
Anonymous, R., , Sunbury Rep. No. 2176, Anglo-Iranian Oil Co., 1943. [all data]

Anonymous, 1942
Anonymous, R., , Am. Pet. Inst. Res. Proj. 6, Natl. Bur. Stand., 1942. [all data]

Carr and Stucklen, 1938
Carr, E.P.; Stucklen, H., The ultraviolet absorbtion of simple hydrocarbons: IV unsaturated cyclic hydrocarbons in the schumann region, J. Chem. Phys., 1938, 6, 55. [all data]

Maess and Mueffling, 1937
Maess, L.; Mueffling, L., The vapor pressure of several hydrocarbons and ketones, Angew. Chem., 1937, 50, 759. [all data]

Maess and von Muffling, 1937
Maess, L.; von Muffling, L., On the Vapor Pressures of Hydrocarbons and Ketones, Angew. Chem., 1937, 50, 759. [all data]

Hofmann, Lang, et al., 1933
Hofmann, F.; Lang, K.F.; Berlin, K.; Schmidt, A.W., Brennst.-Chem., 1933, 14, 103. [all data]

Von Auwers, 1918
Von Auwers, K., Justus Liebigs Ann. Chem., 1918, 415, 98. [all data]

Harries and Tank, 1908
Harries, C.; Tank, L., Ber. Dtsch. Chem. Ges., 1908, 41, 1701. [all data]

Meiser, 1899
Meiser, W., Chem. Ber., 1899, 32, 2049. [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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