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Cycloartane

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Chemical compound
Cycloartane
Names
IUPAC name 9,19-Cyclo-9β-lanostane
Systematic IUPAC name (1R,3aS,3bS,5aS,9aR,10aS,12aR)-3a,6,6,12a-Tetramethyl-1-tetradecahydro-1H,10H-cyclopentacyclopropaphenanthrene
Other names
  • Cycloorthane
  • 9,19-Cyclolanostane
  • 4,4,14-Trimethyl-9,19-cyclo-5alpha,9beta-cholestane
Identifiers
CAS Number
3D model (JSmol)
Beilstein Reference 3207210 3207211
ChEBI
ChemSpider
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C30H52/c1-21(2)10-8-11-22(3)23-14-17-28(7)25-13-12-24-26(4,5)15-9-16-29(24)20-30(25,29)19-18-27(23,28)6/h21-25H,8-20H2,1-7H3/t22-,23-,24+,25+,27-,28+,29-,30+/m1/s1Key: BSLYZLYLUUIFGZ-JRUDBKCSSA-N
SMILES
  • C(CCCC(C)C)1CC2(1(CC342CC53(C4)CCCC5(C)C)C)C
Properties
Chemical formula C30H52
Molar mass 412.746 g·mol
Density 0.95±0.1 g·cm
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Cycloartane is a triterpene, also known as 4,4,14-trimethyl-9,19-cyclo-5alpha,9beta-cholestane. Its derivative cycloartenol is the starting point for the synthesis of almost all plant steroids.

See also

References

  1. Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (© 1994-2019 ACD/Labs). Retrieved from SciFinder.
  2. Schaller, Hubert (May 2003). "The role of sterols in plant growth and development". Progress in Lipid Research. 42 (3): 163–175. doi:10.1016/S0163-7827(02)00047-4. PMID 12689617.


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