Dialkyl ethers
Dialkyl ethers are a class of organic compounds characterized by the presence of two alkyl groups attached to an ether functional group (?O?). These compounds play significant roles in various applications due to their unique chemical properties. Commonly, dialkyl ethers can be derived from alcohols through dehydration reactions or directly synthesized via the reaction between an alcohol and another alcohol in the presence of a strong acid catalyst.
Dialkyl ethers are highly stable under acidic conditions but can undergo hydrolysis when exposed to basic environments. They possess good solvating properties, making them useful as solvents for various organic compounds. Additionally, due to their low water solubility and high vapor pressure, dialkyl ethers serve well in applications requiring specific phase behavior.
In the pharmaceutical industry, certain dialkyl ethers are used as intermediates or excipients. Their chemical inertness and biocompatibility make them suitable for formulating drug delivery systems. In the automotive sector, some dialkyl ethers function as fuel additives to improve engine performance and reduce emissions. Furthermore, in the electronics industry, these compounds find application as dielectric fluids due to their high介電常數(shù)和低揮發(fā)性。
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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(2-Chloroethoxy)methyl Chloride | 1462-33-5 | C3H6Cl2O |
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1-bromo-2-methoxy-2-methylpropane | 19752-21-7 | C5H11BrO |
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Undecanoic acid, 2-[2-(2-hydroxyethoxy)ethoxy]ethyl ester | 62304-84-1 | C17H34O5 |
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Butane, 1,1,1-trichloro-2-methoxy-2-methyl- | 62688-88-4 | C6H11Cl3O |
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1,3-Dichloroisopropyl-2,3-dichloropropyl Ether (>85%) | 59440-90-3 | C6H10Cl4O |
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Cyclohexane,[(1E)-3-ethoxy-1-propen-1-yl]- | 62103-22-4 | C11H20O |
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Butane,1-[2-bromo-1-(bromomethyl)ethoxy]- | 5442-16-0 | C7H14Br2O |
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Ethanol,2-[2-[2-[2-(4-octylphenoxy)ethoxy]ethoxy]ethoxy]- | 51437-92-4 | C22H38O5 |
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Triethylene Glycol Mono(p-nonylphenyl) Ether | 51437-95-7 | C21H36O4 |
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(prop-2-yn-1-yloxy)cyclohexane | 67967-07-1 | C9H14O |
Related Literature
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Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745
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Joseph W. Bennett,Diamond T. Jones,Blake G. Hudson,Joshua Melendez-Rivera,Robert J. Hamers,Sara E. Mason Environ. Sci.: Nano, 2020,7, 1642-1651
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J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
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Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
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Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” Kim Lab Chip, 2009,9, 1732-1739
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