Cyclohexene, 1-methyl-
- Formula: C7H12
- Molecular weight: 96.1702
- IUPAC Standard InChIKey: CTMHWPIWNRWQEG-UHFFFAOYSA-N
- CAS Registry Number: 591-49-1
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
View 3d structure (requires JavaScript / HTML 5) - Other names: α-Methylcyclohexene; 1-Methylcyclohexene; 1-Methyl-1-cyclohexene; 1-Methylcyclohex-1-ene; 1-Methylcyclohexene-1
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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
Tboil (K) | Reference | Comment |
---|---|---|
383.5 | Weast and Grasselli, 1989 | BS |
382. | Samartsev and Ogloblin, 1965 | Uncertainty assigned by TRC = 1. K; TRC |
381. | Brown, Ayyangar, et al., 1964 | Uncertainty assigned by TRC = 2. K; TRC |
383.47 | Anonymous, 1961 | Uncertainty assigned by TRC = 0.3 K; TRC |
383.4 | Turner and Garner, 1958 | Uncertainty assigned by TRC = 0.6 K; TRC |
383. | Blomquist, Verdol, et al., 1957 | Uncertainty assigned by TRC = 2. K; TRC |
381.9 | Cope, Bumgardner, et al., 1957 | Uncertainty assigned by TRC = 3. K; TRC |
381. | Liu, 1956 | Uncertainty assigned by TRC = 4. K; TRC |
382. | Oppenlander and Day, 1956 | Uncertainty assigned by TRC = 4. K; TRC |
383.5 | Anonymous, 1954 | Uncertainty assigned by TRC = 1. K; TRC |
383.45 | Anonymous, 1954, 2 | Uncertainty assigned by TRC = 0.8 K; TRC |
382.3 | Levina, Mezentsova, et al., 1953 | Uncertainty assigned by TRC = 0.6 K; TRC |
384. | Plate, Liberman, et al., 1953 | Uncertainty assigned by TRC = 2. K; TRC |
383.5 | Boord, Henne, et al., 1949 | Uncertainty assigned by TRC = 0.5 K; TRC |
383.45 | Anonymous, 1943 | Uncertainty assigned by TRC = 0.5 K; TRC |
383. | Signaigo and Cramer, 1933 | Uncertainty assigned by TRC = 4. K; TRC |
385. | Ebel, Brunner, et al., 1929 | Uncertainty assigned by TRC = 3. K; TRC |
378. | Gough, Hunter, et al., 1926 | Uncertainty assigned by TRC = 4. K; TRC |
376. | Ipatieff, 1910 | Uncertainty assigned by TRC = 16. K; TRC |
378. | Sabatier and Mailhe, 1905 | Uncertainty assigned by TRC = 5. K; TRC |
382. | Sabatier and Mailhe, 1905 | Uncertainty assigned by TRC = 6. K; TRC |
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]
Brown, Ayyangar, et al., 1964
Brown, H.C.; Ayyangar, N.R.; Zweifel, G.,
Hydroboration XIX. The Reaction of Diisopinocpmpheylborane with Representative trand and Hindered Olefins. Triisopinocampheldiborane as A Reagent for the Configuraional Assignment of Alcohols and Ole,
J. Am. Chem. Soc., 1964, 86, 1071-6. [all data]
Anonymous, 1961
Anonymous, R.,
Preliminary thermodyn. prop. of FREON-14, E. I. Du Pont, Freon Tech. Bull. T-14, 1961. [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]
Blomquist, Verdol, et al., 1957
Blomquist, A.T.; Verdol, J.A.; Adami, C.L.; Wolinsky, J.; Phillips, D.D.,
J. Am. Chem. Soc., 1957, 79, 4976. [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]
Liu, 1956
Liu, Y.-C.,
Free Radical Reaction. Reaction of Grignard Reagents with 2-Bromo-2,3- dimethylbutane and with1-Chloro-1-methylcyclohexane in the presence of Condensed Halides,
Huaxue Xuebao, 1956, 22, 104. [all data]
Oppenlander and Day, 1956
Oppenlander, G.C.; Day, A.R.,
The Structure and Mechanism of FOrmation of Some Cyclogeraniolenes,
J. Org. Chem., 1956, 21, 961-4. [all data]
Anonymous, 1954
Anonymous, R.,
, Am. Pet. Inst. Res. Proj. 45, Tech. Rep. 13, Ohio State Univ., 1954. [all data]
Anonymous, 1954, 2
Anonymous, R.,
Am. Pet. Inst. Res. Proj. 6, 1954, Carnegie-Mellon Univ., March 1954. [all data]
Levina, Mezentsova, et al., 1953
Levina, R.Ya.; Mezentsova, N.N.; Akishin, P.A.,
Contact Isomerization of Unsaturated Hydrocarbons XIX. Isomerization of Unsaturated Five- and Six-membered Cyclic Hydrocarbons with a Double Bond in the Ring or in the Side Chain,
Zh. Obshch. Khim., 1953, 23, 562-9. [all data]
Plate, Liberman, et al., 1953
Plate, A.F.; Liberman, A.L.; Momma, N.A.,
Preparation of 1,2-Dialkylcycloanes. Synthesis of Stereoisomeric 1-Methyl-2-butylcyclopentanes,
Izv. Akad. Nauk SSSR, 1953, 1953, 689. [all data]
Boord, Henne, et al., 1949
Boord, C.E.; Henne, A.L.; Greenlee, K.W.; Perilstein, W.L.; Derfer, J.M.,
The Grignard Reagent in hydrocarbon synthesis,
Ind. Eng. Chem., 1949, 41, 609. [all data]
Anonymous, 1943
Anonymous, R.,
, Sunbury Rep. No. 2176, Anglo-Iranian Oil Co., 1943. [all data]
Signaigo and Cramer, 1933
Signaigo, F.K.; Cramer, P.L.,
The preparation of some mono- and dialkylcylohexanes,
J. Am. Chem. Soc., 1933, 55, 3326-32. [all data]
Ebel, Brunner, et al., 1929
Ebel, F.; Brunner, R.; Mangelli, P.,
Norcarane,
Helv. Chim. Acta, 1929, 12, 19. [all data]
Gough, Hunter, et al., 1926
Gough, G.A.C.; Hunter, H.; Kenyon, J.,
The alcohols of the hydroaromatic and terpene series: V the geometrical and optical isomerism of the methylcyclohexanols.,
J. Chem. Soc., 1926, 129, 2052-71. [all data]
Ipatieff, 1910
Ipatieff, W.,
Chem. Ber., 1910, 43, 3383. [all data]
Sabatier and Mailhe, 1905
Sabatier, P.; Mailhe, A.,
C. R. Hebd. Seances Acad. Sci., 1905, 140, 350. [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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