Introduction：Basic information about macrocarpal J CAS 179603-47-5, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
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 |
Safety Information
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
