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CAS NO.225110-25-8
| Falcarindiol Basic information |
| Product Name: | Falcarindiol |
| Synonyms: | (3R,8S)-Falcarindiol;3(R),8(S),9(Z)-Falcarindiol;(3R,8S,9Z)-1,9-Heptadecadiene-4,6-diyne-3,8-diol;1,9-Heptadecadiene-4,6-diyne-3,8-diol,(3R,8S,9Z)- |
| CAS: | 225110-25-8 |
| MF: | C17H24O2 |
| MW: | 260.37126 |
| EINECS: | |
| Product Categories: | Aliphatics;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals |
| Mol File: | 225110-25-8.mol |
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| Falcarindiol Chemical Properties |
| Safety Information |
| Falcarindiol Usage And Synthesis |
| Usage | Falcarindiol was isolated as an algicidal principle against the harmful red tide dinoflagellate, Heterocapsa circularisquama, from Notopterygii Rhizoma through bioassay-guided separation.To determine the ambiguous absolute structure of this active principle, all three stereoisomers as well as falcarindiol were synthesized. As a result of intensive analytical of their physicochemical properties, the configuration of Falcarinfiol was revealed to be 3R,8S. (3S,8S)- and (3S,8R)-isomers were found to exhibit more potent algicidal activity than (3R,8S)-Falcarindiol isolated from Notopterygii Rhizoma. |
| Falcarindiol Basic information |
| Product Name: | Falcarindiol |
| Synonyms: | (3R,8S)-Falcarindiol;3(R),8(S),9(Z)-Falcarindiol;(3R,8S,9Z)-1,9-Heptadecadiene-4,6-diyne-3,8-diol;1,9-Heptadecadiene-4,6-diyne-3,8-diol,(3R,8S,9Z)- |
| CAS: | 225110-25-8 |
| MF: | C17H24O2 |
| MW: | 260.37126 |
| EINECS: | |
| Product Categories: | Aliphatics;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals |
| Mol File: | 225110-25-8.mol |
|
|
|
| Falcarindiol Chemical Properties |
| Safety Information |
| Falcarindiol Usage And Synthesis |
| Usage | Falcarindiol was isolated as an algicidal principle against the harmful red tide dinoflagellate, Heterocapsa circularisquama, from Notopterygii Rhizoma through bioassay-guided separation.To determine the ambiguous absolute structure of this active principle, all three stereoisomers as well as falcarindiol were synthesized. As a result of intensive analytical of their physicochemical properties, the configuration of Falcarinfiol was revealed to be 3R,8S. (3S,8S)- and (3S,8R)-isomers were found to exhibit more potent algicidal activity than (3R,8S)-Falcarindiol isolated from Notopterygii Rhizoma. |