Glycoperine

Base Information

Chemical Name:Glycoperine
CAS No.:55740-45-9
Molecular Formula:C₁₉H₂₁NO₈
Molecular Weight:391.378
Hs Code.:
DSSTox Substance ID:DTXSID70331999
Nikkaji Number:J12.410I
Wikidata:Q27106776
Metabolomics Workbench ID:69507
Mol file:55740-45-9.mol

Synonyms:Glycoperine;55740-45-9;(2S,3R,4R,5R,6S)-2-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-6-methyloxane-3,4,5-triol;C10686;AC1L9DM8;starbld0000881;CHEBI:5479;STOCK1N-21976;DTXSID70331999;MolPort-002-513-217;HY-N7478;ZINC03984166;AKOS030492227;CS-0129872;Q27106776;(2S,3R,4R,5R,6S)-2-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-6-methyl-tetrahydropyran-3,4,5-triol

Suppliers and Price of Glycoperine

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

ChemScene
Glycoperine
1mg
$ 950.00

Total 5 raw suppliers

Chemical Property of Glycoperine

Chemical Property:

Vapor Pressure:1.5E-15mmHg at 25°C
Boiling Point:606.3°C at 760 mmHg
Flash Point:320.5°C
PSA：123.64000
Density:1.448g/cm³
LogP:1.20450
XLogP3:1.2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:4
Exact Mass:391.12671663
Heavy Atom Count:28
Complexity:538

Purity/Quality:

97% ^*data from raw suppliers

Glycoperine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)O)O)O
Isomeric SMILES:C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=C(C3=C(C=C2)C(=C4C=COC4=N3)OC)OC)O)O)O
Description A glycosidic alkaloid of the furanoquinoline type, glycoperine occurs in the extract from Haplophyllum perforatum. The structure has been established from a study of the infrared, ultraviolet, NMR and mass spectra.

Technology Process of Glycoperine

There total 2 articles about Glycoperine 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: