Jump to content

Ciclotic acid

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Vanished user 0x8cSXE0x6 (talk | contribs) at 12:21, 16 December 2016. The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Ciclotic acid
Names
IUPAC name
4-methylbicyclo[2.2.2]oct-2-ene-1-carboxylic acid
Other names
Ciclotic acid, ciclotate, cyclotate
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=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-
    Key: AMMPLVWPWSYRDR-MGCOHNPYSA-N
  • C[C@@]12C=C[C@@](CC1)(CC2)C(=O)O
Properties
C10H13O2
Molar mass 165.21 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

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

References

  1. ^ http://apps.who.int/medicinedocs/documents/s20132en/s20132en.pdf
  2. ^ https://www.google.com/patents/US3458505
  3. ^ J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 660–. ISBN 978-1-4757-2085-3.
  4. ^ Index Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 1473–. ISBN 978-3-88763-075-1.