| 词条 | Methoxyethane |
| 释义 |
| SMILES = COCC | CASNo_Ref = {{cascite|correct|??}} | CASNo = 540-67-0 | PubChem = 10903 | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | ChemSpiderID = 10441 | ChEBI_Ref = {{ebicite|changed|EBI}} | ChEBI = 39832 | InChI = 1/C3H8O/c1-3-4-2/h3H2,1-2H3 | InChIKey = XOBKSJJDNFUZPF-UHFFFAOYAP | StdInChI_Ref = {{stdinchicite|changed|chemspider}} | StdInChI = 1S/C3H8O/c1-3-4-2/h3H2,1-2H3 | StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} | StdInChIKey = XOBKSJJDNFUZPF-UHFFFAOYSA-N | C=3 | H=8 | O=1 | Appearance = Colorless gas[2] | Density = 0.7251 g cm−3 (at 0 °C)[2] | Solubility = | MeltingPtC = -113 | BoilingPtC = 7.4 | RefractIndex = 1.3420 (at 4 °C)[2] | pKa = | pKb = | Viscosity = 0.224 cP at 25 °C | MolShape = | Dipole = | ExternalSDS = External MSDS | MainHazards = Extremely Flammable (F+), Liquefied gas |Section8={{Chembox Related | OtherFunction_label = Ethers | OtherFunction = Dimethyl ether Diethyl ether Methoxypropane }} }} Methoxyethane, also known as ethyl methyl ether, is a colorless gaseous ether with a medicine-like odor. It is extremely flammable, and its inhalation may cause asphyxiation or dizziness. As a Lewis base, it can react with Lewis acids to form salts and reacts violently with oxidizing agents. References1. ^{{cite book | title = Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book) | publisher = The Royal Society of Chemistry | date = 2014 | location = Cambridge | page = 703 | doi = 10.1039/9781849733069-00648 | isbn = 978-0-85404-182-4}} {{Molecules detected in outer space}}{{Authority control}}{{organic-compound-stub}}2. ^1 2 {{CRC91|page=3-248}} 2 : Dialkyl ethers|Ether solvents |
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