2,4-Hexadiene, 2,5-dimethyl-
- Formula: C8H14
- Molecular weight: 110.1968
- IUPAC Standard InChI: InChI=1S/C8H14/c1-7(2)5-6-8(3)4/h5-6H,1-4H3
- IUPAC Standard InChIKey: DZPCYXCBXGQBRN-UHFFFAOYSA-N
- CAS Registry Number: 764-13-6
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Other names: Biisobutenyl; Biisocrotyl; Diisocrotyl; 2,5-Dimethyl-2,4-hexadiene; (CH3)2C=CHCH=C(CH3)2; 2,5-Dimethylhexa-2,4-diene; NSC 10812
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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 |
|---|---|---|
| 406.2 | Aldrich Chemical Company Inc., 1990 | BS |
| 405. to 407. | Farchan Laboratories, 1990 | BS |
| 407.7 | Weast and Grasselli, 1989 | BS |
| 382. | Kotlyarevskii and Zanina, 1957 | Uncertainty assigned by TRC = 10. K; TRC; Data excluded from overall average |
| 407.7 | Gostunskaya and Kazanskii, 1955 | Uncertainty assigned by TRC = 0.5 K; TRC |
| 407.2 | Yur'ev, Kondrat'eva, et al., 1952 | Uncertainty assigned by TRC = 2. K; TRC |
| 407.5 | Kazanskii and Gostunskaya, 1950 | Uncertainty assigned by TRC = 0.6 K; TRC |
| 407.7 | Boord, Henne, et al., 1949 | Uncertainty assigned by TRC = 0.5 K; TRC |
| 407.65 | Boord, Greenlee, et al., 1946 | Uncertainty assigned by TRC = 0.5 K; TRC |
| 407.7 | Cleveland, 1944 | Uncertainty assigned by TRC = 0.5 K; TRC |
| 407.7 | Henne and Chanan, 1944 | Uncertainty assigned by TRC = 0.5 K; TRC |
| 407.7 | Henne and Turk, 1942 | Uncertainty assigned by TRC = 0.5 K; TRC |
| 407.65 | Anonymous, 1941 | Uncertainty assigned by TRC = 0.3 K; TRC |
| 407.7 | Turk, 1941 | Uncertainty assigned by TRC = 0.5 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.
Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc.,
Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]
Farchan Laboratories, 1990
Farchan Laboratories,
Research Chemicals Catalog, Farchan Laboratories, Gainesville, FL, 1990, 91. [all data]
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]
Kotlyarevskii and Zanina, 1957
Kotlyarevskii, I.L.; Zanina, A.S.,
Unsaturated Hydrocarbons V. Synthesis of p-Xylene,
Zh. Prikl. Khim. (Leningrad), 1957, 30, 1356-6. [all data]
Gostunskaya and Kazanskii, 1955
Gostunskaya, I.V.; Kazanskii, B.A.,
Zh. Obshch. Khim., 1955, 25, 1995. [all data]
Yur'ev, Kondrat'eva, et al., 1952
Yur'ev, Y.; Kondrat'eva, G.Y.; Akishin, P.A.; Derbeneva,
Zh. Obshch. Khim., 1952, 22, 339. [all data]
Kazanskii and Gostunskaya, 1950
Kazanskii, B.A.; Gostunskaya, I.V.,
Dokl. Akad. Nauk SSSR, 1950, 71, 295. [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]
Boord, Greenlee, et al., 1946
Boord, C.E.; Greenlee, K.W.; Perilstein, W.L.,
The Synthesis, Purification and Prop. of Hydrocarbons of Low Mol. Weight, Am. Pet. Inst. Res. Proj. 45, Eighth Annu. Rep., Ohio State Univ., June 30, 1946. [all data]
Cleveland, 1944
Cleveland, F.F.,
J. Chem. Phys., 1944, 12, 53. [all data]
Henne and Chanan, 1944
Henne, A.L.; Chanan, H.H.,
Diolefins from Allylic Chlorides II.,
J. Am. Chem. Soc., 1944, 66, 392. [all data]
Henne and Turk, 1942
Henne, A.L.; Turk, A.,
Conjugated diolefins by double bond displacement,
J. Am. Chem. Soc., 1942, 64, 826-8. [all data]
Anonymous, 1941
Anonymous, R.,
, Am. Pet. Inst. Hydrocarbon Res. Proj., Third Annu. Rep., Ohio State Univ., Aug. 31, 1941. [all data]
Turk, 1941
Turk, A.,
, Ph.D. Thesis, Ohio State Univ., Columbus, OH, 1941. [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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