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225110-25-8

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225110-25-8 Usage

Uses

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.

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.

225110-25-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-(3R,8S)-falcarindiol

1.2 Other means of identification

Product number -
Other names Falcarindiol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:225110-25-8 SDS

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

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