225110-25-8 Usage
Description
Falcarindiol is a naturally occurring compound that has been isolated as an algicidal principle against the harmful red tide dinoflagellate, Heterocapsa circularisquama. It is derived from Notopterygii Rhizoma through bioassay-guided separation. The compound has been synthesized in three stereoisomers, with the configuration of Falcarindiol being 3R,8S. It is known for its potent algicidal activity, with some isomers exhibiting more potent effects than others.
Uses
Used in Algal Control:
Falcarindiol is used as an algicide for controlling harmful algal blooms, particularly against the red tide dinoflagellate, Heterocapsa circularisquama. Its algicidal activity helps in mitigating the negative impacts of algal blooms on aquatic ecosystems and human health.
Used in Chemical Research:
Falcarindiol is used as a subject of study in chemical research to determine its ambiguous absolute structure and to understand the differences in activity between its various stereoisomers. This research contributes to the development of more effective and targeted algicides for controlling harmful algal blooms.
Used in Environmental Protection:
Falcarindiol is used in environmental protection efforts to combat the detrimental effects of harmful algal blooms on aquatic ecosystems, marine life, and human health. Its algicidal properties make it a valuable tool in managing and preventing the spread of red tide events and other harmful algal blooms.
Check Digit Verification of cas no
The CAS Registry Mumber 225110-25-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,1,1 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 225110-25:
(8*2)+(7*2)+(6*5)+(5*1)+(4*1)+(3*0)+(2*2)+(1*5)=78
78 % 10 = 8
So 225110-25-8 is a valid CAS Registry Number.
225110-25-8Relevant articles and documents
Stereoselective approaches for the total synthesis of polyacetylenic (3R,8S)-falcarindiol
Sabitha, Gowravaram,Bhaskar, Vangala,Reddy, Ch. Srinivas,Yadav, Jhillu S.
, p. 115 - 121 (2008)
The total synthesis of the polyacetylenic compound falcarindiol was achieved by two different routes from a common intermediate. Georg Thieme Verlag Stuttgart.
Establishment of absolute stereostructure of falcarindiol, algicidal principle against Heterocapsa circularisquama from Notopterygii Rhizoma
Tamura, Satoru,Ohno, Tomomichi,Hattori, Yuuhi,Murakami, Nobutoshi
scheme or table, p. 1523 - 1525 (2010/04/29)
Falcarindiol (1) was isolated as an algicidal principle against the harmful red tide dinoflagellate, Heterocapsa circularisquama, from Notopterygii Rhizoma through bioassay-guided separation. In order to determine the ambiguous absolute structure of this
