亞甲基環己烷

亞甲基環己烷
	IUPAC名; Methylidenecyclohexane
別名	Methylenecyclohexane
識別
CAS號	1192-37-6
PubChem	14502
ChemSpider	13846
SMILES	C=C1CCCCC1;
InChI	1/C7H12/c1-7-5-3-2-4-6-7/h1-6H2;
InChIKey	YULMNMJFAZWLLN-UHFFFAOYAJ
性質
化學式	C7H12
摩爾質量	96.170 g·mol⁻¹
密度	0.8074 g·cm−3（20 °C）
熔點	−106.7 °C（166.5 K）
沸點	102—103 °C（375—376 K）
溶解性（水）	0.083 g/L
	若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。

亞甲基環己烷是一種有機化合物，化學式為C₇H₁₂，是難溶於水的無色液體。它可由Wittig反應，或由環己酮和Tebbe試劑反應製得。^[5]^[6]^[7]它和二氧化硫作用，異構為1-甲基環己烯。^[8]

參考文獻

^ Arthur I. Vogel. 250. Physical properties and chemical constitution. Part III. cycloPentane, cyclohexane, cycloheptane, and some derivatives. The multiplanar structure of the methylcyclohexane ring. Journal of the Chemical Society (Resumed). 1938: 1323 [2019-12-04]. ISSN 0368-1769. doi:10.1039/jr9380001323 （英語）.
^ "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFinder. [2019-12-4]
^ Fawarsky, Al.; Borgmann, I. Isomeric Rearrangement. Berichte der Deutschen Chemischen Gesellschaft, 1908. 40: 4863-4875. ISSN: 0365-9496.
^ Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (© 1994-2019 ACD/Labs). Retrieved from SciFinder. [2019-12-4]
^ Wittig, George; Schoellkopf, U. Methylenecyclohexane. Organic Syntheses. 1960, 40: 66 [2019-12-04]. doi:10.15227/orgsyn.040.0066. （原始內容存檔於2019-11-07）.
^ Mark, Herman F. Encyclopedia of Polymer Science and Technology, Concise. Hoboken, New Jersey: John Wiley & Sons. 2007: 682 [2019-12-04]. ISBN 978-0-470-04610-4. （原始內容存檔於2019-03-06）. I this way, cyclohexanone is transformed into methylenecyclohexene and benzaldehyde into stryene.
^ Dalton, David R. Foundations of Organic Chemistry: Unity and Diversity of Structures, Pathways, and Reactions. John Wiley & Sons. August 4, 2011: 819–820 [2019-12-04]. ISBN 978-1-118-00538-5. （原始內容存檔於2019-03-06）. Now, when cyclohexanone is added to the solution in which the [Tebbe] reagent has been generated, reaction occurs to produce methylenecyclohexane and triphenylphosphine oxide
^ Divakar Masilamani, Edward H. Manahan, John Vitrone, Milorad M. Rogic. Organic reactions of sulfur dioxide. Reactions with nucleophilic double bonds leading to the isomerization, aromatization, selective hydrogen-deuterium exchange, and electron-transfer processes. The Journal of Organic Chemistry. 1983-12, 48 (25): 4918–4931 [2019-12-04]. ISSN 0022-3263. doi:10.1021/jo00173a028 （英語）.

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[1] Arthur I. Vogel. 250. Physical properties and chemical constitution. Part III. cycloPentane, cyclohexane, cycloheptane, and some derivatives. The multiplanar structure of the methylcyclohexane ring. Journal of the Chemical Society (Resumed). 1938: 1323 [2019-12-04]. ISSN 0368-1769. doi:10.1039/jr9380001323 （英語）.

[2] "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFinder. [2019-12-4]

[3] Fawarsky, Al.; Borgmann, I. Isomeric Rearrangement. Berichte der Deutschen Chemischen Gesellschaft, 1908. 40: 4863-4875. ISSN: 0365-9496.

[4] Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (© 1994-2019 ACD/Labs). Retrieved from SciFinder. [2019-12-4]

[5] Wittig, George; Schoellkopf, U. Methylenecyclohexane. Organic Syntheses. 1960, 40: 66 [2019-12-04]. doi:10.15227/orgsyn.040.0066. （原始內容存檔於2019-11-07）.

[6] Mark, Herman F. Encyclopedia of Polymer Science and Technology, Concise. Hoboken, New Jersey: John Wiley & Sons. 2007: 682 [2019-12-04]. ISBN 978-0-470-04610-4. （原始內容存檔於2019-03-06）. I this way, cyclohexanone is transformed into methylenecyclohexene and benzaldehyde into stryene.

[7] Dalton, David R. Foundations of Organic Chemistry: Unity and Diversity of Structures, Pathways, and Reactions. John Wiley & Sons. August 4, 2011: 819–820 [2019-12-04]. ISBN 978-1-118-00538-5. （原始內容存檔於2019-03-06）. Now, when cyclohexanone is added to the solution in which the [Tebbe] reagent has been generated, reaction occurs to produce methylenecyclohexane and triphenylphosphine oxide

[8] Divakar Masilamani, Edward H. Manahan, John Vitrone, Milorad M. Rogic. Organic reactions of sulfur dioxide. Reactions with nucleophilic double bonds leading to the isomerization, aromatization, selective hydrogen-deuterium exchange, and electron-transfer processes. The Journal of Organic Chemistry. 1983-12, 48 (25): 4918–4931 [2019-12-04]. ISSN 0022-3263. doi:10.1021/jo00173a028 （英語）.

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