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Eleutheroside B1

Base Information
  • Chemical Name:Eleutheroside B1
  • CAS No.:16845-16-2
  • Molecular Formula:C17H20O10
  • Molecular Weight:384.34
  • Hs Code.:
  • UNII:AZA7PP6D4R
  • DSSTox Substance ID:DTXSID801316838
  • Nikkaji Number:J1.452.997G
Eleutheroside B1

Synonyms:Eleutheroside B1;16845-16-2;Eleutheroside-B1;ELEUTHEROSIDE B1(RG);AZA7PP6D4R;UNII-AZA7PP6D4R;Isofraxidin alpha-D-glucopyranoside;Isofraxidin 7-o-alpha-D-glucopyranoside;2H-1-Benzopyran-2-one, 7-(alpha-D-glucopyranosyloxy)-6,8-dimethoxy-;7-(alpha-D-Glucopyranosyloxy)-6,8-dimethoxy-2H-1-benzopyran-2-one;6,8-dimethoxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one;DTXSID801316838;AKOS040760770;AC-34064;MS-26315;HY-135646;CS-0113675;ISOFRAXIDIN .ALPHA.-D-GLUCOPYRANOSIDE;E80556;ISOFRAXIDIN 7-O-.ALPHA.-D-GLUCOPYRANOSIDE;2H-1-BENZOPYRAN-2-ONE, 7-(.ALPHA.-D-GLUCOPYRANOSYLOXY)-6,8-DIMETHOXY-;7-(.ALPHA.-D-GLUCOPYRANOSYLOXY)-6,8-DIMETHOXY-2H-1-BENZOPYRAN-2-ONE;6,8-Dimethoxy-7-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-2H-chromen-2-one

Suppliers and Price of Eleutheroside B1
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
Total 19 raw suppliers
Chemical Property of Eleutheroside B1
Chemical Property:
  • Boiling Point:675.0±55.0 °C(Predicted) 
  • PKA:12.65±0.70(Predicted) 
  • PSA:148.05000 
  • Density:1.524±0.06 g/cm3(Predicted) 
  • LogP:-1.01110 
  • XLogP3:-0.3
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:10
  • Rotatable Bond Count:5
  • Exact Mass:384.10564683
  • Heavy Atom Count:27
  • Complexity:554
Purity/Quality:

≥98% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)OC3C(C(C(C(O3)CO)O)O)O
  • Isomeric SMILES:COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O
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