USD $1.00-1.00 / Kilogram
USD $1.00-1.00 / Kilogram
USD $48.00-58.00 / Kilogram
USD $6.00-9.00 / Gram
USD $1.00-10.00 / Kilogram
USD $1.00-1.00 / Kilogram
USD $4.50-5.00 / Liter
USD $4.50-5.00 / Liter
USD $4.50-5.00 / Liter
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. |
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. |