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macrocarpal J

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Products Intro: Product Name:Macrocarpal J
CAS:179603-47-5
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Products Intro: Product Name:Macrocarpal J
CAS:179603-47-5
Purity:95% Package:100g; 1kg Remarks:LN03247898
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Products Intro: Product Name:Macrocarpal J
CAS:179603-47-5
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Products Intro: Product Name:Macrocarpal J
CAS:179603-47-5
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Products Intro: Product Name:Macrocarpal J
CAS:179603-47-5
Purity:97.0% Package:5mg Remarks:BBP01756
macrocarpal J Basic information
Product Name:macrocarpal J
Synonyms:macrocarpal J;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-[(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
CAS:179603-47-5
MF:C28H42O7
MW:490.63
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Mol File:179603-47-5.mol
macrocarpal J Structure
macrocarpal J Chemical Properties
Boiling point 569.5±50.0 °C(Predicted)
density 1.226±0.06 g/cm3(Predicted)
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form powder
pka5.40±0.50(Predicted)
color Yellow
Safety Information
MSDS Information
macrocarpal J Usage And Synthesis
UsesMacrocarpal J, a phloroglucinol sesquiterpene-coupled compound, can be isolated from the leaves of Eucalyptus globulus.
targetAntifection
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. DOI:10.1021/np9604994
macrocarpal J Preparation Products And Raw materials
Tag:macrocarpal J(179603-47-5) Related Product Information
2-(3,4-Dihydroxyphenyl)-8-(2-O-beta-L-galactopyranosyl-beta-D-glucopyranosyl)-5,7-dihydroxy-4H-1-Benzopyran-4-one hydroxygenkwanin (4E,6E)-1,7-Diphenyl-4,6-heptadien-3-one alpha-Terpineol MOSLOFLAVONE beta-Sitosterol Artemether beta-Eudesmol Hydroxyecdysone alpha-Cyperone macrocarpal H Macrocarpal K Macrocarpal E Macrocarpal N Macrocarpal D macrocarpal I

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