2-甲基四氢呋喃
一般危化品
2-甲基四氢呋喃结构式
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常用名 | 2-甲基四氢呋喃 | 英文名 | 2-Methyltetrahydrofuran |
|---|---|---|---|---|
| CAS号 | 96-47-9 | 分子量 | 86.132 | |
| 密度 | 0.9±0.1 g/cm3 | 沸点 | 79.9±0.0 °C at 760 mmHg | |
| 分子式 | C5H10O | 熔点 | -136 °C | |
| MSDS | 中文版 美版 | 闪点 | -11.1±0.0 °C | |
| 符号 |
GHS02, GHS05, GHS07 |
信号词 | Danger |
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On-line monitoring of continuous flow chemical synthesis using a portable, small footprint mass spectrometer.
J. Am. Soc. Mass Spectrom. 25(10) , 1794-802, (2014) For on-line monitoring of chemical reactions (batch or continuous flow), mass spectrometry (MS) can provide data to (1) determine the fate of starting materials and reagents, (2) confirm the presence of the desired product, (3) identify intermediates and impu... |
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Efficient synthesis of phosphatidylserine in 2-methyltetrahydrofuran.
J. Biotechnol. 163(1) , 45-9, (2013) 2-Methyltetrahydrofuran has recently been described as a promising and green solvent. Herein, it was successfully used as the reaction medium for enzyme-mediated transphosphatidylation of phosphatidylcholine with L-serine with the aim of phosphatidylserine sy... |
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Temperature dependence of charge separation and recombination in porphyrin oligomer-fullerene donor-acceptor systems.
J. Am. Chem. Soc. 133(25) , 9863-71, (2011) Electron-transfer reactions are fundamental to many practical devices, but because of their complexity, it is often very difficult to interpret measurements done on the complete device. Therefore, studies of model systems are crucial. Here the rates of charge... |
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2-methyltetrahydrofuran--lithium hexafluoroarsenate: a superior electrolyte for the secondary lithium electrode.
Science 204(4392) , 499-501, (1979) Rechargeable, high energy density lithium batteries require an efficient lithium electrode. Earlier work with electrolytes based on propylene carbonate, methyl acetate, and tetrahydrofuran yielded poor lithium electrode cycling efficiencies because of electro... |
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2-Methyltetrahydrofuran (2-MeTHF): A Biomass-Derived Solvent with Broad Application in Organic Chemistry. Pace V, et al.
ChemSusChem 5(8) , 1369-1379, (2012)
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Solvent applications of 2-methyltetrahydrofuran in organometallic and biphasic reactions. Aycock DF.
Org. Process Res. Dev. 11(1) , 156-159, (2007)
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Regiocontrolled ring opening of 2-methyltetrahydrofuran with acid chlorides and iodides. Mimero P, et al.
Tetrahedron Lett. 35(10) , 1553-1556, (1994)
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Enzyme-catalyzed C-C bond formation using 2-methyltetrahydrofuran (2-MTHF) as (co) solvent: efficient and bio-based alternative to DMSO and MTBE. Shanmuganathan S, et al.
Green Chem. 12(12) , 2240-2245, (2010)
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Efficient chemoselective addition of Grignard reagents to carbonyl compounds in 2-methyltetrahydrofuran. Zhong W, et al.
J. Chem. Res. (M) 2009(6) , 370-373, (2009)
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2-Methyltetrahydrofuran as an alternative to dichloromethane in 2-phase reactions. Ripin DHB and Vetelino M.
Synlett 15 , 2353-2353, (2003)
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