Coumarin or 2H-chromen-2-one is an aromatic organic chemical compound with formula.
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Coumarin or 2H-chromen-2-one is an aromatic organic chemical compound with formula.
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Coumarin is a colorless crystalline solid with a sweet odor resembling the scent of vanilla and a bitter taste.
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Coumarin is derived from coumarou, the French word for the tonka bean.
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Coumarin was first isolated from tonka beans in 1820 by A Vogel of Munich, who initially mistook it for benzoic acid.
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Coumarin was first synthesized in 1868 by the English chemist William Henry Perkin.
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Coumarin has been an integral part of the fougere genre of perfume since it was first used in Houbigant's Fougere Royale in 1882.
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Coumarin can be prepared by a number of name reactions, with the Perkin reaction between salicylaldehyde and acetic anhydride being a popular example.
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Coumarin is found naturally in many edible plants such as strawberries, black currants, apricots, and cherries.
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Coumarin is transformed into the natural anticoagulant dicoumarol by a number of species of fungi.
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Coumarin is used in the pharmaceutical industry as a precursor reagent in the synthesis of a number of synthetic anticoagulant pharmaceuticals similar to dicoumarol.
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Coumarin dyes are extensively used as gain media in blue-green tunable organic dye lasers.
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Coumarin is often found in artificial vanilla substitutes, despite having been banned as a food additive in numerous countries since the mid-20th century.
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Coumarin was banned as a food additive in the United States in 1954, largely because of the hepatotoxicity results in rodents.
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Coumarin is currently listed by the Food and Drug Administration of the United States among "Substances Generally Prohibited From Direct Addition or Use as Human Food, " according to 21 CFR 189.
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Coumarin held that from a chemist's point of view, coumarin is an “immediate precursor” to the rodenticide coumadin.
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