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・ Cyclopentadienylmolybdenum tricarbonyl dimer
・ Cyclopentadienylthallium
・ Cyclopentamine
・ Cyclopentane
・ Cyclopentanepentone
・ Cyclopentanol
・ Cyclopentanol dehydrogenase
・ Cyclopentanone
・ Cyclopentanone monooxygenase
・ Cyclopentene
・ Cyclopentenone
・ Cyclopentenone prostaglandin
・ Cyclopenthiazide
・ Cyclopentobarbital
・ Cyclopentolate
Cyclopentyl methyl ether
・ Cyclopeplus
・ Cyclopeplus batesi
・ Cyclopeplus castaneus
・ Cyclopeplus cyaneus
・ Cyclopeplus lacordairei
・ Cyclopeplus peruvianus
・ Cyclopera
・ Cyclopes
・ Cyclophane
・ Cyclopharynx
・ Cyclophile Aigle
・ Cyclophilin
・ Cyclophiops
・ Cyclophiops doriae


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Cyclopentyl methyl ether : ウィキペディア英語版
Cyclopentyl methyl ether

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Cyclopentyl methyl ether (CPME), also known as methoxy cyclopentane, it is hydrophobic ether solvent. A high boiling point (106 °C) and preferable characteristics such as low formation of peroxides, relative stability under acidic and basic conditions, formation of azeotropes with water coupled with a narrow explosion range render CPME an alternative to other ethereal solvents such as tetrahydrofuran (THF), 2-methyl tetrahydrofuran (2-MeTHF), dioxane (carcinogenic), and 1,2-dimethoxyethane (DME).
== Synthesis ==
The synthesis of this compound can be done in two different ways:
(1) by methylation of the cyclopentanol.
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(2) by the addition of methanol to the cyclopentene. This second method is better from the point of view of sustainable chemistry since it does not produce by-products.
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抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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