{"type":"standard","title":"Picene","displaytitle":"Picene","namespace":{"id":0,"text":""},"wikibase_item":"Q3180495","titles":{"canonical":"Picene","normalized":"Picene","display":"Picene"},"pageid":3133155,"thumbnail":{"source":"https://upload.wikimedia.org/wikipedia/commons/thumb/d/d8/Picene.svg/320px-Picene.svg.png","width":320,"height":229},"originalimage":{"source":"https://upload.wikimedia.org/wikipedia/commons/thumb/d/d8/Picene.svg/218px-Picene.svg.png","width":218,"height":156},"lang":"en","dir":"ltr","revision":"1237718814","tid":"dee1406f-4ef6-11ef-8e2b-474bb06b9e9d","timestamp":"2024-07-31T04:39:28Z","description":"Chemical compound","description_source":"local","content_urls":{"desktop":{"page":"https://en.wikipedia.org/wiki/Picene","revisions":"https://en.wikipedia.org/wiki/Picene?action=history","edit":"https://en.wikipedia.org/wiki/Picene?action=edit","talk":"https://en.wikipedia.org/wiki/Talk:Picene"},"mobile":{"page":"https://en.m.wikipedia.org/wiki/Picene","revisions":"https://en.m.wikipedia.org/wiki/Special:History/Picene","edit":"https://en.m.wikipedia.org/wiki/Picene?action=edit","talk":"https://en.m.wikipedia.org/wiki/Talk:Picene"}},"extract":"Picene is a hydrocarbon found in the pitchy residue obtained in the distillation of peat tar and of petroleum. This is distilled to dryness and the distillate repeatedly recrystallized from cymene. It may be synthetically prepared by the action of anhydrous aluminium chloride on a mixture of naphthalene and 1,2-dibromoethane, or by distilling a-dinaphthostilbene. It crystallizes in large colorless plates which possess a blue fluorescence. It is soluble in concentrated sulfuric acid with a green color. Chromic acid in glacial acetic acid solution oxidizes it to picene-quinone, picene-quinone carboxylic acid, and finally to phthalic acid.","extract_html":"
Picene is a hydrocarbon found in the pitchy residue obtained in the distillation of peat tar and of petroleum. This is distilled to dryness and the distillate repeatedly recrystallized from cymene. It may be synthetically prepared by the action of anhydrous aluminium chloride on a mixture of naphthalene and 1,2-dibromoethane, or by distilling a-dinaphthostilbene. It crystallizes in large colorless plates which possess a blue fluorescence. It is soluble in concentrated sulfuric acid with a green color. Chromic acid in glacial acetic acid solution oxidizes it to picene-quinone, picene-quinone carboxylic acid, and finally to phthalic acid.
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{"fact":"In just seven years, a single pair of cats and their offspring could produce a staggering total of 420,000 kittens.","length":115}
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