Chrysanthemic acid

Chrysanthemic acid
Names
IUPAC name
2,2-Dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylic acid
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.022.788
  • 16747 (1R,3R) or (+)-trans
  • 33607 (1S,3S) or (−)-trans
  • 33606 (1R,3S) or (+)-cis
  • 20755 (1S,3R) or (−)-cis
UNII
  • InChI=1S/C10H16O2/c1-6(2)5-7-8(9(11)12)10(7,3)4/h5,7-8H,1-4H3,(H,11,12)/t7-,8+/m0/s1
    Key: XLOPRKKSAJMMEW-JGVFFNPUSA-N
  • CC(=CC1C(C1(C)C)C(=O)O)C
Properties
C10H16O2
Molar mass 168.236 g·mol−1
Melting point 17 °C (63 °F; 290 K) (1R,3R) or (+)-trans
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Chrysanthemic acid is an organic compound that is related to a variety of natural and synthetic insecticides. It is related to the pyrethrin I and II, as well as the pyrethroids. One of the four stereoisomers, (1R,3R)- or (+)-trans-chrysanthemic acid (pictured), is the acid part of the ester pyrethrin I, which occurs naturally in the seed cases of Chrysanthemum cinerariaefolium. Many synthetic pyrethroids, for example the allethrins, are esters of all four stereoisomers. Staudinger and Ružička named chrysanthemic acid in 1924.