CAS:225110-25-8 C17...

CAS:225110-25-8 C17H24O2 Falcarindiol

CAS:225110-25-8 C17H24O2 Falcarindiol

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500 Gram

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  • Min.Order :500 Gram
  • Purity: 99%
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Keywords

CAS:225110-25-8 C17H24O2 Falcarindiol CAS:225110-25-8 C17H24O2 CAS:225110-25-8

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  • Appearance:white poweder
  • Application:CAS:225110-25-8 C17H24O2 Falcarindiol
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  • ProductionCapacity:1|Metric Ton|Day
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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 Structure
 
Falcarindiol Chemical Properties
 
Safety Information
MSDS 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.

 

Details:

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 Structure
 
Falcarindiol Chemical Properties
 
Safety Information
MSDS 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.

 

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