Falcarindiol

Base Information

Chemical Name:Falcarindiol
CAS No.:225110-25-8
Molecular Formula:C17H24O2
Molecular Weight:260.376
Hs Code.:
Mol file:225110-25-8.mol

Synonyms:(+)-(3R,8S)-Falcarindiol;(3R),(8S)-Falcarindiol;3(R),8(S),9(Z)-Falcarindiol;

Suppliers and Price of Falcarindiol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(3R,8S)-Falcarindiol
10mg
$ 10725.00

JR MediChem
Falcarindiol(NewProduct) 98%
20mg
$ 468.00

DC Chemicals
Falcarindiol >98%,StandardReferencesGrade
20 mg
$ 280.00

CSNpharm
(+)-(3R,8S)-Falcarindiol
5mg
$ 213.00

CSNpharm
(+)-(3R,8S)-Falcarindiol
10mg
$ 362.00

Crysdot
(+)-(3R,8S)-Falcarindiol 95+%
5mg
$ 450.00

Crysdot
(+)-(3R,8S)-Falcarindiol 95+%
10mg
$ 680.00

AvaChem
Falcarindiol
20mg
$ 690.00

AvaChem
Falcarindiol
1mg
$ 119.00

AvaChem
Falcarindiol
5mg
$ 290.00

Total 38 raw suppliers

Chemical Property of Falcarindiol

Chemical Property:

Boiling Point:408.2 °C at 760 mmHg
PKA:11.65±0.20(Predicted)
Flash Point:184.8 °C
PSA：40.46000
Density:1 g/cm³
LogP:2.81770

Purity/Quality:

97% ^*data from raw suppliers

(3R,8S)-Falcarindiol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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.

Technology Process of Falcarindiol

There total 10 articles about Falcarindiol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 87.0%

: 1013028-70-0
(3R,8S,9Z)-8-(tert-butyldimethylsiloxy)heptadeca-1,9-diene-4,6-diyn-3-ol

: 225110-25-8
(3R,8S)-falcarindiol

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 1h;
DOI:10.1055/s-2007-990944

Reference yield: 83.9%

: 224636-41-3
(3R,8S)-3-(tert-butyldiphenylsilyloxy)falcarindiol

: 225110-25-8
(3R,8S)-falcarindiol

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃; for 3h;
DOI:10.1021/np980418z

Reference yield:

: 224636-40-2
(S,Z)‐dodec‐4‐en‐1‐yn‐3‐ol

: 72800-75-0
(R)-5-bromo-1-penten-4-yn-3-ol

: 225110-25-8
(3R,8S)-falcarindiol

Guidance literature:: With hydroxylamine hydrochloride; N-butylamine; copper(l) chloride; In methanol; dichloromethane; at 0 ℃; for 3h; Darkness; Inert atmosphere;
DOI:10.1002/anie.201302538