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Forsythoside B

Base Information
  • Chemical Name:Forsythoside B
  • CAS No.:81525-13-5
  • Molecular Formula:C34H44O19
  • Molecular Weight:756.70200
  • Hs Code.:29389090
  • Mol file:81525-13-5.mol
Forsythoside B

Synonyms:Forsythoside B;

Suppliers and Price of Forsythoside B
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
  • Usbiological
  • Forsythoside B
  • 20mg
  • $ 490.00
  • TRC
  • ForsythosideB
  • 250mg
  • $ 745.00
  • JR MediChem
  • ForsythosideB 98%
  • 20mg
  • $ 1000.00
  • DC Chemicals
  • ForsythosideB >98%
  • 250 mg
  • $ 900.00
  • CSNpharm
  • ForsythosideB
  • 10mg
  • $ 115.00
  • Crysdot
  • ForsythosideB 95+%
  • 250mg
  • $ 750.00
  • Crysdot
  • ForsythosideB 95+%
  • 50mg
  • $ 225.00
  • Crysdot
  • ForsythosideB 95+%
  • 100mg
  • $ 375.00
  • Crysdot
  • ForsythosideB 95+%
  • 5mg
  • $ 45.00
  • Crysdot
  • ForsythosideB 95+%
  • 10mg
  • $ 70.00
Total 57 raw suppliers
Chemical Property of Forsythoside B
Chemical Property:
  • Boiling Point:1040.3±65.0 °C(Predicted) 
  • PKA:9.31±0.10(Predicted) 
  • PSA:304.21000 
  • Density:1.65 
  • LogP:-2.55100 
  • Storage Temp.:2-8°C 
  • Solubility.:Methanol (Slightly) 
Purity/Quality:

≥98% *data from raw suppliers

Forsythoside B *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses Forsythoside B is an anti-inflammatory agent protecting against such effects such as sepsis. Neuroprotective agent.
Refernces

Phenylpropanoid glycosides from Lamiophlomis rotata

10.1016/S0031-9422(99)00027-8

The study focuses on the isolation and structural identification of two new phenylpropanoid glycosides, 6'-β-D-apiofuranosyl cistanoside C and cis-lamiophlomiside A, from the roots of Lamiophlomis rotata, a plant used in traditional Chinese medicine. The research utilized spectral and chemical evidence to determine the structures of the compounds, which were found to be similar to known compounds like lamiophlomiside A, alyssonoside, and forsythoside B. The study also involved the hydrolysis of compound 2, leading to the identification of its sugar components, and permethylation of compound 2 and lamiophlomiside A to confirm their structural similarities. The findings contribute to the understanding of the phytochemical constituents of L. rotata and their potential applications in medicine.

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