| 词条 | Carvonic acid |
| 释义 |
| Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 428751289 | ImageFile = Carvonic acid.svg | IUPACName = 2-(4-Methyl-5-oxo-cyclohex-3-enyl)-acrylic acid | OtherNames = |Section1={{Chembox Identifiers | CASNo_Ref = {{cascite|correct|??}} | CASNo = 362483-06-5 | CASNo_Comment = (racemate) | SMILES = CC1=CC[C@H](CC1=O)C(=C)C(=O)O | SMILES_Comment = (R) | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | ChemSpiderID = 27330306 | ChemSpiderID_Comment = (R) | StdInChI_Ref = {{stdinchicite|changed|chemspider}} | StdInChI = 1S/C10H12O3/c1-6-3-4-8(5-9(6)11)7(2)10(12)13/h3,8H,2,4-5H2,1H3,(H,12,13)/t8-/m1/s1 | StdInChI_Comment = (R) | StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} | StdInChIKey = BPJKNHQCPHBIAR-MRVPVSSYSA-N | ChemSpiderID1_Ref = {{chemspidercite|changed|chemspider}} | ChemSpiderID1 = 27330305 | ChemSpiderID1_Comment = (S) | PubChem = 71308172 | SMILES1 = CC1=CC[C@@H](CC1=O)C(=C)C(=O)O | SMILES1_Comment = (S) | InChI3 = 1S/C10H12O3/c1-6-3-4-8(5-9(6)11)7(2)10(12)13/h3,8H,2,4-5H2,1H3,(H,12,13)/t8-/m0/s1 | InChI3_Comment = (S) | InChIKey3 = BPJKNHQCPHBIAR-QMMMGPOBSA-N |Section2={{Chembox Properties | Formula = C10H12O3 | MolarMass = 180.20 g/mol | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }}Carvonic acid, or α-methylene-4-methyl-5-oxo-3-cyclohexene-1-acetic acid, is a terpenoid formed by metabolism of carvone in humans.[1] References1. ^{{cite journal| author = Engel, W. | title = In Vivo Studies on the Metabolism of the Monoterpenes S-(+)- and R-(−)-Carvone in Humans Using the Metabolism of Ingestion-Correlated Amounts (MICA) Approach | journal = J. Agric. Food Chem.| year = 2001| volume = 49| issue = 8| pages = 4069–4075| doi = 10.1021/jf010157q| pmid=11513712}} {{ketone-stub}} 4 : Carboxylic acids|Monoterpenes|Ketones|Cyclohexenes |
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