Icariside F2

Base Information

Chemical Name:Icariside F2
CAS No.:115009-57-9
Molecular Formula:C18H26 O10
Molecular Weight:402.398
Hs Code.:
European Community (EC) Number:802-514-8
ChEMBL ID:CHEMBL3326712
Metabolomics Workbench ID:131260
Nikkaji Number:J668.685K
Wikidata:Q76423577
Mol file:115009-57-9.mol

Synonyms:Icariside F2;115009-57-9;(2R,3S,4S,5R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-phenylmethoxyoxane-3,4,5-triol;benzyl acuminose;CHEMBL3326712;CHEBI:181622;HY-N8085;AKOS040760081;NCGC00385106-01;Icariside F2, >=90% (LC/MS-ELSD);CS-0139924;Benzyl 6-O-beta-D-apiofuranosyl-beta-D-glucoside;benzyl 6-O-beta-D-apiofuranosyl-beta-D-glucopyranoside;NCGC00385106-01_C18H26O10_beta-D-Glucopyranoside, phenylmethyl 6-O-[(2R,3R,4R)-tetrahydro-3,4-dihydroxy-4-(hydroxymethyl)-2-furanyl]-

Suppliers and Price of Icariside F2

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

Sigma-Aldrich
Icariside F2 ≥90% (LC/MS-ELSD)
1mg
$ 365.00

Total 9 raw suppliers

Chemical Property of Icariside F2

Chemical Property:

PSA：158.30000
LogP:-2.53200
Storage Temp.:?20°C
XLogP3:-2.3
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:7
Exact Mass:402.15259702
Heavy Atom Count:28
Complexity:487

Purity/Quality:

Analysis control,98.0% ^*data from raw suppliers

Icariside F2 ≥90% (LC/MS-ELSD) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi
Statements: 36
Safety Statements: 26

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O
Isomeric SMILES:C1[C@@]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O

Technology Process of Icariside F2

There total 9 articles about Icariside F2 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: 100.0%

: benzyl 2,3,4-tri-O-acetyl-6-O-<(3-C-acetoxymethyl)-2,3-di-O-acetyl-β-D-erythrofuranosyl>-β-D-glucopyranoside

: 115009-57-9
icariside F₂

Guidance literature:: With sodium methylate; In methanol; for 1h; Ambient temperature;
DOI:10.1016/0008-6215(94)80057-X

Reference yield: 23.0%

: benzyl 6-O-(2,3-O-isopropylidene-β-D-apiofuranosyl)-β-D-glucopyranoside

: 115009-57-9
icariside F₂

Guidance literature:: With trifluoroacetic acid; at 20 ℃; for 0.166667h;

Reference yield:

: 2,3,4-tri-O-acetyl-6-O-<(3-C-acetoxymethyl)-2,3-di-O-acetyl-β-D-erythrofuranosyl>-α-D-glucopyranosyl trichloroacetimidate

: 115009-57-9
icariside F₂

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / BF₃*Et₂O / CH₂Cl₂ / Ambient temperature

2: 100 percent / MeONa / methanol / 1 h / Ambient temperature

With boron trifluoride diethyl etherate; sodium methylate; In methanol; dichloromethane;
DOI:10.1016/0008-6215(94)80057-X