274-40-8c1ccn2cccc2c1HOBCFUWDNJPFHB-UHFFFAOYSA-NIndolizine is a mancude organic heterobicyclic parent and a member of indolizines.
274-40-8DTXSID50181818CHEMBL3622747CHEBI:35583安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
Warning
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 4 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
解説C8H7N(117.15).ピロコリンともいう.2-ピコリンとブロモピルビン酸エチルから得られるインドリジン-2-カルボン酸を脱炭酸して合成される."板状晶.融点75 ℃,沸点205 ℃.ナフタレン臭をもち,水蒸気蒸留される.普通の有機溶媒に可溶.ベンゼン溶液は紫色の蛍光をもつ.[CAS 274-40-8]森北出版「化学辞典(第2版)
使用Indolizine is a useful chemical intermediate
純化方法Purify indolizine through an alumina column in *C6H6 and elute with *C6H6 (toluene could be used instead). The eluate contained in the fluorescent band (using UV light 365mn) is collected, evaporated and the crystalline residue is sublimed twice at 40-50o/0.2-0.5mm. The colourless crystals darken on standing and should be stored in dark sealed containers. If the original sample is dark in color then it should be covered with water and steam distilled. The colourless crystals in the distillate are collected and dried between filter paper and sublimed. It protonates on C3 in aqueous acid. It should give one fluorescent spot on paper chromatography (Whatman 1) in 3% aqueous ammonia and in n-BuOH/AcOH/H2O (4:1:1). The picrate has m 101o from EtOH. [Armarego J Chem Soc 226 1964, Armarego J Chem Soc (B) 191 1966, Scholtz Chem Ber 45 734 1912, Beilstein 20 II 200, 20 III/IV 3195.]
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