| 词条 | Norcamphor |
| 释义 |
| ImageFile = Norcamphor.svg | ImageSize = 150px | IUPACName = Bicyclo[2.2.1]heptan-2-one | OtherNames = 2-Norbornanone |Section1={{Chembox Identifiers | CASNo = 497-38-1 | PubChem = 10345 | ChemSpiderID = 9919 | ChEMBL = 361682 | SMILES = O=C1CC2CC1CC2 | InChI = 1/C7H10O/c8-7-4-5-1-2-6(7)3-5/h5-6H,1-4H2 | InChIKey = KPMKEVXVVHNIEY-UHFFFAOYAC | StdInChI = 1S/C7H10O/c8-7-4-5-1-2-6(7)3-5/h5-6H,1-4H2 | StdInChIKey = KPMKEVXVVHNIEY-UHFFFAOYSA-N |Section2={{Chembox Properties | C=7 | H=10 | O=1 | Appearance = Colorless solid | Density = | MeltingPtC = 93 to 96 | MeltingPt_ref = [1] | BoilingPtC = 168 to 172 | BoilingPt_ref = [1] | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }}Norcamphor is an organic compound, classified as a bicyclic ketone. It is an analog of camphor, but without the three methyl groups. A colorless solid, it is used as a building block in organic synthesis. Norcamphor is prepared from norbornene via the 2-formate ester, which is oxidized. It is a useful precursor to norborneols.[2] See also
References1. ^1 {{cite web | title = Norcamphor | url = http://www.sigmaaldrich.com/catalog/product/aldrich/n32601?lang=en | publisher = Sigma-Aldrich | accessdate = March 11, 2013}} {{ketone-stub}}2. ^{{cite journal |first=Donald C. |last=Kleinfelter |first2=Paul von R. |last2=Schleyer |title=2-Norbornanone |journal=Org. Synth. |year=1962 |volume=42 |issue= |pages=79 |doi=10.15227/orgsyn.042.0079 }} 2 : Ketones|Cyclopentanes |
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