1,1-二乙氧基环己烷
1,1-二乙氧基环己烷结构式
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常用名 | 1,1-二乙氧基环己烷 | 英文名 | Cyclohexane,1,1-diethoxy- |
|---|---|---|---|---|
| CAS号 | 1670-47-9 | 分子量 | 172.26500 | |
| 密度 | 0.908 g/mL at 25 °C(lit.) | 沸点 | 76-78 °C20 mm Hg(lit.) | |
| 分子式 | C10H20O2 | 熔点 | N/A | |
| MSDS | 中文版 美版 | 闪点 | 140 °F | |
| 符号 |
GHS02, GHS07 |
信号词 | Warning |
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Kinetics and mechanisms of the unimolecular elimination of 2,2-diethoxypropane and 1,1-diethoxycyclohexane in the gas phase: experimental and theoretical study.
J. Phys. Chem. A 116(2) , 846-54, (2012) The gas-phase thermal elimination of 2,2-diethoxypropane was found to give ethanol, acetone, and ethylene, while 1,1-diethoxycyclohexane yielded 1-ethoxycyclohexene and ethanol. The kinetics determinations were carried out, with the reaction vessels deactivat... |
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Catecholborane (1, 3, 2-benzodioxaborole). A versatile reducing agent. Kabalka GW, et al.
J. Org. Chem. 42(3) , 512-517, (1977)
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Reactions of Enol Ethers with Carbenes. V. Rearrangements of Dihalocyclopropanes Derived from Six-, Seven-, and Eight-Membered Cyclic Enol Ethers1. Parham WE, et al.
J. Am. Chem. Soc. 87(2) , 321-328, (1965)
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Ozonolysis-reductive amination of olefins. Pollart KA and Miller RE.
J. Org. Chem. 27(7) , 2392-2394, (1962)
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