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  • BioBioPha
  • China
  • Product Name: Murraol
  • Price: ¥3600.0/5mg
  • Purity: 98.0%
  • Stocking Period: 10 Day
  • Contact: Xueping-Zheng


  • DC Chemicals Limited
  • China
  • Product Name: Murraol
  • Price: $Inquiry/100mg $Inquiry/250mg $Inquiry/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

109741-38-0

109741-38-0 structure
109741-38-0 structure
  • Name: Murraol
  • Chemical Name: 8-[(1E)-3-Hydroxy-3-methyl-1-buten-1-yl]-7-methoxy-2H-chromen-2-o ne
  • CAS Number: 109741-38-0
  • Molecular Formula: C15H16O4
  • Molecular Weight: 260.285
  • Catalog: Natural product Coumarin
  • Create Date: 2017-03-07 17:25:01
  • Modify Date: 2024-01-06 15:44:34
  • Murraol (CM-c2), a coumarin, can be isolated from the leaves of Madagascar pine cork (Apiaceae). Murraol has cyclooxygenase (COX) and lipoxygenase inhibitory properties and has an inhibitory effect on the growth of cancer cells[1].

Name 8-[(1E)-3-Hydroxy-3-methyl-1-buten-1-yl]-7-methoxy-2H-chromen-2-o ne
Synonyms 2H-1-Benzopyran-2-one, 8-[(1E)-3-hydroxy-3-methyl-1-buten-1-yl]-7-methoxy-
7-ethoxy-3,7-dimethyl-2-octen-1-ol
7-Ethoxygeraniol
8-[(1E)-3-Hydroxy-3-methyl-1-buten-1-yl]-7-methoxy-2H-chromen-2-one
Description Murraol (CM-c2), a coumarin, can be isolated from the leaves of Madagascar pine cork (Apiaceae). Murraol has cyclooxygenase (COX) and lipoxygenase inhibitory properties and has an inhibitory effect on the growth of cancer cells[1].
Related Catalog
References

[1]. Riviere C, et al. Antiproliferative effects of isopentenylated coumarins isolated from Phellolophium madagascariense Baker. Nat Prod Res. 2006 Aug;20(10):909-16.  

Density 1.2±0.1 g/cm3
Boiling Point 466.9±45.0 °C at 760 mmHg
Molecular Formula C15H16O4
Molecular Weight 260.285
Flash Point 176.7±22.2 °C
Exact Mass 260.104858
PSA 59.67000
LogP 2.04
Vapour Pressure 0.0±1.2 mmHg at 25°C
Index of Refraction 1.604
Hazard Codes Xi

~27%

109741-38-0 structure

109741-38-0

Literature: Reisch, Johannes; Bathe, Andreas Liebigs Annalen der Chemie, 1988 , p. 543 - 548

~%

109741-38-0 structure

109741-38-0

Literature: Ito; Furukawa Chemical and Pharmaceutical Bulletin, 1989 , vol. 37, # 3 p. 819 - 820
Precursor  3

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