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| | 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 | | EINECS: | | | Product Categories: | | | Mol File: | 179603-47-5.mol |  |
| | 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 | | pka | 5.40±0.50(Predicted) | | color | Yellow |
| | macrocarpal J Usage And Synthesis |
| Uses | Macrocarpal J, a phloroglucinol sesquiterpene-coupled compound, can be isolated from the leaves of Eucalyptus globulus. | | target | Antifection | | 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 |
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