| 词条 | Ciclotic acid |
| 释义 |
| ImageFile = Ciclotic acid.png | ImageSize = | ImageAlt = | IUPACName = 4-methylbicyclo[2.2.2]oct-2-ene-1-carboxylic acid | OtherNames = Ciclotic acid, ciclotate, cyclotate | Section1 = {{Chembox Identifiers | CASNo = | ChemSpiderID = 58178411 | SMILES = C[C@@]12C=C[C@@](CC1)(CC2)C(=O)O | StdInChI = 1S/C10H14O2/c1-9-2-5-10(6-3-9,7-4-9)8(11)12/h2,5H,3-4,6-7H2,1H3,(H,11,12)/t9-,10- | StdInChIKey = AMMPLVWPWSYRDR-MGCOHNPYSA-N | Section2 = {{Chembox Properties | C=10 | H=13 | O=2 | MolarMass = 165.21 g/mol | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }}Ciclotic acid, or cyclotic acid, systematic name 4-methylbicyclo[2.2.2]oct-2-ene-1-carboxylic acid, is a bicyclic carboxylic acid.[1] The salts and esters of ciclotic acid are known as ciclotates (cyclotates). An example is nandrolone cyclotate, a long-acting ester prodrug of the anabolic-androgenic steroid nandrolone.[2][3][4] See also
References1. ^http://apps.who.int/medicinedocs/documents/s20132en/s20132en.pdf {{organic-compound-stub}}2. ^https://www.google.com/patents/US3458505 3. ^{{cite book|author=J. Elks|title=The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies|url=https://books.google.com/books?id=0vXTBwAAQBAJ&pg=PA660|date=14 November 2014|publisher=Springer|isbn=978-1-4757-2085-3|pages=660–}} 4. ^{{cite book|title=Index Nominum 2000: International Drug Directory|url=https://books.google.com/books?id=5GpcTQD_L2oC&pg=PA1473|date=January 2000|publisher=Taylor & Francis|isbn=978-3-88763-075-1|pages=1473–}} 1 : Cyclohexanecarboxylic acids |
| 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。