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Tetrahydrofuran (THF), or oxolane, is an organic compound with the formula (CH 2) 4 O. The compound is classified as heterocyclic compound , specifically a cyclic ether . It is a colorless, water- miscible organic liquid with low viscosity .
It is dissimilar vs ethers such as tetrahydrofuran. Like enol ethers, 2,5-disubstituted furans are susceptible to hydrolysis to reversibly give 1,4-diketones. Furan serves as a diene in Diels–Alder reactions with electron-deficient dienophiles such as ethyl ( E )-3-nitroacrylate. [ 15 ]
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Deuterated tetrahydrofuran (d 8-THF) is a colourless, organic liquid at standard temperature and pressure. [1] This heterocyclic compound has the chemical formula C 4 D 8 O, and is an isotopologue of tetrahydrofuran. [2] Deuterated THF is used as a solvent in NMR spectroscopy, though its expense can often be prohibitive. [citation needed]
There are many physiologic changes that occur during pregnancy that influence respiratory status and function. Progesterone has noticeable effects on respiratory physiology, increasing minute volume (the amount of air breathed in and out of the lungs in 1 minute) by 40% in the first trimester via an increase in tidal volume alone, as the ...
It is produced by polymerization of tetrahydrofuran as well as 1,4-butanediol. The product is commercially available as polymers of low average molecular weights , between 250 and 3000 daltons . In this form it is a white waxy solid that melts between 20 and 30 °C.
Borane–tetrahydrofuran is an adduct derived from borane and tetrahydrofuran (THF). These solutions, which are colorless, are used for reductions and hydroboration , reactions that are useful in synthesis of organic compounds .
These hormones have essential functions in pregnancy test, maintaining the uterine lining, fetal development, preventing premature labor, and the initiation and support of labor. Subsequently, the hormones are stored and released into the circulation to be conveyed to the specific cells they are intended for.