
呋喃 - 维基百科,自由的百科全书
呋喃(英語: furan ,IUPAC:oxole) [1] ,化学用名氧杂茂 [2] [3] 或𫫇茂 [需明示出處] ,是一种五元芳香性 杂环 有机物,其五元环含有四个碳 原子、一个氧原子和两个环内共轭双键,并具有类似于苯环的6个π电子大共轭体系 [4] 。
Furan - 110-00-9, C4H4O, density, melting point, boiling point ...
2024年4月29日 · Furan - cas 110-00-9, synthesis, structure, density, melting point, boiling point
Furan - Wikipedia
Furan is a heterocyclic organic compound, consisting of a five-membered aromatic ring with four carbon atoms and one oxygen atom. Chemical compounds containing such rings are also referred to as furans. Furan is a colorless, flammable, highly volatile liquid with a boiling point close to room temperature.
呋喃 - 百度百科
呋喃(oxole),是最简单的含氧五元杂环化合物,化学式为C4H4O,它存在于松木焦油中,为无色液体,具有类似氯仿的气味,难溶于水,易溶于有机溶剂。它的蒸气遇有被盐酸浸湿过的松木片时,即呈现绿色,叫做松木反应,可用来鉴定呋喃的存在。它有麻醉和弱刺激作用,极度易燃。吸 …
Furan | C4H4O | CID 8029 - PubChem
Furan | C4H4O | CID 8029 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
呋喃_化工百科 - ChemBK
中文名:呋喃,英文名:Furan,CAS:110-00-9,化学式:C4H4O,分子量:68.07,密度:0.936 g/mL at 25 °C(lit.),熔点:-85.6 °C,沸点:67°C10mm Hg(lit.),闪点:160°F,水溶性:insoluble,蒸汽压:1672 mm Hg ( 55 °C),折射率:n20/D 1.5070(lit.),MSDS.
Furan | Synthesis, Polymerization, Reactions | Britannica
furan, any of a class of organic compounds of the heterocyclic aromatic series characterized by a ring structure composed of one oxygen atom and four carbon atoms. The simplest member of the furan family is furan itself, a colourless, volatile, and …
Furan - an overview | ScienceDirect Topics
Furan is a five-member heterocyclic aromatic organic compound consisting of four carbon and one oxygen atoms. From: Chemistry of 2-Oxoaldehydes and 2-Oxoacids, 2022
Furans - Chemistry Online
2024年4月22日 · furan is a colorless, highly volatile and flammable liquid with a boiling point of 31 ºC. It is also slightly soluble in water, soluble in common organic solvents, and with a dipole moment μ = 0.72 Debye. It has an odor similar to chloroform. The ring system of furan is found in many natural compounds, is toxic and may be carcinogenic in humans.
Synthesis, Reactions and Medicinal Uses of Furan
2024年4月17日 · During protonation, electron-releasing substituents on furan generate reactive electrophiles that activate polymerization and lead to ring-opening reactions. Mercuration - Mercuration is an easy process for furan. Reduction - A simple furan cannot be reduced to a tetrahydrofuran without opening its ring. It is possible to decompose furoic acid ...