Names | |
---|---|
IUPAC name
9,19-Cyclo-9β-lanostane
| |
Systematic IUPAC name
(1R,3aS,3bS,5aS,9aR,10aS,12aR)-3a,6,6,12a-Tetramethyl-1-[(2R)-6-methylheptan-2-yl]tetradecahydro-1H,10H-cyclopenta[a]cyclopropa[e]phenanthrene | |
Other names
| |
Identifiers | |
3D model (
JSmol)
|
|
3207210 3207211 | |
ChEBI | |
ChemSpider | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C30H52 | |
Molar mass | 412.746 g·mol−1 |
Density | 0.95±0.1 g·cm−3 [1] |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
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. [2]
Names | |
---|---|
IUPAC name
9,19-Cyclo-9β-lanostane
| |
Systematic IUPAC name
(1R,3aS,3bS,5aS,9aR,10aS,12aR)-3a,6,6,12a-Tetramethyl-1-[(2R)-6-methylheptan-2-yl]tetradecahydro-1H,10H-cyclopenta[a]cyclopropa[e]phenanthrene | |
Other names
| |
Identifiers | |
3D model (
JSmol)
|
|
3207210 3207211 | |
ChEBI | |
ChemSpider | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C30H52 | |
Molar mass | 412.746 g·mol−1 |
Density | 0.95±0.1 g·cm−3 [1] |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
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. [2]