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72715-02-7

72715-02-7 structure
72715-02-7 structure
  • Name: Ilicol
  • Chemical Name: (1R,4aR,7R)-7-(3-Hydroxy-1-propen-2-yl)-1,4a-dimethyldecahydro-1- naphthalenol
  • CAS Number: 72715-02-7
  • Molecular Formula: C15H26O2
  • Molecular Weight: 238.37
  • Catalog: Natural product Sesquiter
  • Create Date: 2017-02-19 08:09:49
  • Modify Date: 2024-01-05 15:50:53
  • Ilicol is a natural product isolated from the roots of Saussurea lappa Clarke. Ilicol inhibits root growth and shows IC50 values of 1.22, 2.90, 7.35, 8.07 mM against P. miliaceum , A. sativa, L. sativa , and R. sativus, respectively. Ilicol reduces Allium cepa cell division without chromosome aberration[1].

Name (1R,4aR,7R)-7-(3-Hydroxy-1-propen-2-yl)-1,4a-dimethyldecahydro-1- naphthalenol
Synonyms ilicic alcohol
2-Naphthaleneethanol, decahydro-8-hydroxy-4a,8-dimethyl-β-methylene-, (2R,4aR,8R)-
Gilvocacin V
(1R,4aR,7R)-7-(3-Hydroxy-1-propen-2-yl)-1,4a-dimethyldecahydro-1-naphthalenol
2-Naphthaleneethanol, decahydro-8-hydroxy-4a,8-dimethyl-β-methylene-, (2R,4aR,8R,8aR)-
(1R,4aR,7R)-7-(3-hydroxyprop-1-en-2-yl)-1,4a-dimethyldecahydronaphthalen-1-ol
gilvocarcin V
(1R,4aR,7R,8aR)-7-(3-Hydroxy-1-propen-2-yl)-1,4a-dimethyldecahydro-1-naphthalenol
Description Ilicol is a natural product isolated from the roots of Saussurea lappa Clarke. Ilicol inhibits root growth and shows IC50 values of 1.22, 2.90, 7.35, 8.07 mM against P. miliaceum , A. sativa, L. sativa , and R. sativus, respectively. Ilicol reduces Allium cepa cell division without chromosome aberration[1].
Related Catalog
References

[1]. Diaz Napal GN, et al. Phytotoxicity of secondary metabolites isolated from Flourensia oolepis S.F.Blake. Chem Biodivers. 2013;10(7):1295-1304.  

Density 1.0±0.1 g/cm3
Boiling Point 350.9±25.0 °C at 760 mmHg
Molecular Formula C15H26O2
Molecular Weight 238.37
Flash Point 158.5±17.8 °C
Exact Mass 238.193283
PSA 40.46000
LogP 3.34
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.515
Hazard Codes Xi

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72715-02-7 structure

72715-02-7

Literature: Guerreiro,E. et al. Phytochemistry (Elsevier), 1979 , vol. 18, p. 1235 - 1237
Precursor  1

DownStream  0