| 词条 | Fluoroacetaldehyde |
| 释义 |
| ImageFile = Fluoroacetaldehyde.svg | ImageSize = 150px | IUPACName = Fluoroacetaldehyde | OtherNames = |Section1={{Chembox Identifiers | CASNo = 1544-46-3 | PubChem = 73766 | ChemSpiderID = 66406 | ChEBI = 14272 | KEGG = C15488 | SMILES = C(C=O)F | InChI = 1/C2H3FO/c3-1-2-4/h2H,1H2 | InChIKey = YYDWYJJLVYDJLV-UHFFFAOYAE | StdInChI = 1S/C2H3FO/c3-1-2-4/h2H,1H2 | StdInChIKey = YYDWYJJLVYDJLV-UHFFFAOYSA-N |Section2={{Chembox Properties | C=2 | H=3 | F=1 | O=1 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }}Fluoroacetaldehyde is a metabolic precursor of both fluoroacetate and 4-fluorothreonine in Streptomyces cattleya.[1] References1. ^{{cite journal |author1=Steven J. Moss |author2=Cormac D. Murphy |author3=John T. G. Hamilton |author4=W. Colin McRoberts |author5=David O’Hagan |author6=Christoph Schaffrath |author7=David B. Harper | date = 2000 | title = Fluoroacetaldehyde: a precursor of both fluoroacetateand 4-fluorothreonine in Streptomyces cattleya | journal = Chemical Communications | issue = 22 | pages = 2281–2282 | doi = 10.1039/B007261N}} 3 : Organofluorides|Aldehydes|Fluorine-containing natural products |
| 随便看 |
|
开放百科全书收录14589846条英语、德语、日语等多语种百科知识，基本涵盖了大多数领域的百科知识，是一部内容自由、开放的电子版国际百科全书。