词条 | Apoatropine |
释义 |
| ImageFile = Apoatropine.svg | ImageSize = 200px | IUPACName = (8-Methyl-8-azabicyclo[3.2.1]octan-3-yl) 2-phenylprop-2-enoate | OtherNames = Apoatropine Hydrochloride, Atropamin Hydrochloride, Atropyltropeine Hydrochloride, Apoascyamine, and Atropane. | Section1 = {{Chembox Identifiers | CASNo = 207-906-7 | PubChem = 64695 | SMILES = CN1C2CCC1CC(C2)OC(=O)C(=C)C3=CC=CC=C3 | InChI = InChI=1S/C17H21NO2/c1-12(13-6-4-3-5-7-13)17(19)20-16-10-14-8-9-15(11-16)18(14)2/h3-7,14-16H,1,8-11H2,2H3 [1] | InChIKey = WPUIZWXOSDVQJU-UHFFFAOYSA-N | Section2 = {{Chembox Properties | C=17 | H=21 | N=1 | O=2 | Appearance = White or off whiteish and crystalline | Density = | MeltingPt = >236 °C | MeltingPt_notes = (HCl salt, decomposes)[2] | BoilingPt = | Solubility = Soluble in water, alcohol, and ether | Section3 = {{Chembox Hazards | MainHazards = Considered poisonous | FlashPtC = | AutoignitionPt = }} Apoatropine is a member of class of tropane alkaloids. Apoatropine can be found in plants of Solanaceae family. It is a bitter crystalline alkaloid. Examples of related tropane alkaloids include atropine, hyoscyamine, and hyoscine. Though apoatropine is found in various plants, it can also be prepared by the dehydration of atropine using nitric acid . Apoatropine is used as a pigment.{{cn|date=November 2018}} References1. ^{{cite web|url=https://pubchem.ncbi.nlm.nih.gov/compound/64695#section=Top|title=Apoatropine|author=Pubchem|work=nih.gov}} {{alkaloid-stub}}2. ^{{cite web | url = https://www.scbt.com/scbt/product/apoatropine-hydrochloride | title = Apoatropine Hydrochloride | publisher = Santa Cruz Biotechnology}} 1 : Tropane alkaloids found in Solanaceae |
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