macrocarpal J

Modify Date: 2025-08-25 14:59:19

macrocarpal J Structure
macrocarpal J structure
Common Name macrocarpal J
CAS Number 179603-47-5 Molecular Weight 490.629
Density 1.2±0.1 g/cm3 Boiling Point 569.5±50.0 °C at 760 mmHg
Molecular Formula C28H42O7 Melting Point N/A
MSDS N/A Flash Point 312.2±26.6 °C

 Use of macrocarpal J


Macrocarpal J, a phloroglucinol?sesquiterpene-coupled compound, can be isolated from the leaves of Eucalyptus globulus[1].

 Names

Name 2,4,6-trihydroxy-5-[(1S)-1-[(4S)-4-hydroxy-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-1,2,3,4a,5,6,7,8-octahydronaphthalen-1-yl]-3-methylbutyl]benzene-1,3-dicarbaldehyde
Synonym More Synonyms

 macrocarpal J Biological Activity

Description Macrocarpal J, a phloroglucinol?sesquiterpene-coupled compound, can be isolated from the leaves of Eucalyptus globulus[1].
Related Catalog
References

[1]. Osawa K, et al. Macrocarpals H, I, and J from the Leaves of Eucalyptus globulus. J Nat Prod. 1996 Sep;59(9):823-7.  

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 569.5±50.0 °C at 760 mmHg
Molecular Formula C28H42O7
Molecular Weight 490.629
Flash Point 312.2±26.6 °C
Exact Mass 490.293060
PSA 135.29000
LogP 7.49
Vapour Pressure 0.0±1.6 mmHg at 25°C
Index of Refraction 1.600

 Safety Information

Hazard Codes Xi

 Synonyms

1,3-Benzenedicarboxaldehyde, 5-[(1S)-1-[(1S,4R,4aR,6R,8aS)-decahydro-4-hydroxy-6-(1-hydroxy-1-methylethyl)-4,8a-dimethyl-1-naphthalenyl]-3-methylbutyl]-2,4,6-trihydroxy-
2,4,6-Trihydroxy-5-{(1S)-1-[(1S,4R,4aR,6R,8aS)-4-hydroxy-6-(2-hydroxy-2-propanyl)-4,8a-dimethyldecahydro-1-naphthalenyl]-3-methylbutyl}isophthalaldehyde
Macrocarpal J
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