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Scabioside C

Base Information
  • Chemical Name:Scabioside C
  • CAS No.:17233-22-6
  • Molecular Formula:C41H66O13
  • Molecular Weight:766.95500
  • Hs Code.:
Scabioside C

Synonyms:WE-941;Scabioside C;Leontosid B;Brotizolamum [INN-Latin];[3H]-Brotizolam;2-bromo-4-(2-chlorophenyl)-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine;leontoside B;Lendormin(R);Lendormin;Lendorm;2-Brom-4-(2-chlorphenyl)-9-methyl-6H-thieno<3,2-f><1,2,4>triazolo<4,3-a>1,4>diazepin;

Suppliers and Price of Scabioside C
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
  • Scabioside C
  • 5mg
  • $ 864.00
  • AvaChem
  • Scabioside C
  • 5mg
  • $ 490.00
  • Arctom
  • ScabiosideC;LeontosideB ≥98%
  • 5mg
  • $ 927.27
  • ApexBio Technology
  • ScabiosideC
  • 5mg
  • $ 800.00
Total 14 raw suppliers
Chemical Property of Scabioside C
Chemical Property:
  • Melting Point:242-244℃ 
  • Boiling Point:881.9±65.0 °C(Predicted) 
  • PKA:4.63±0.70(Predicted) 
  • PSA:215.83000 
  • Density:1.35±0.1 g/cm3 (20 oC 760 Torr) 
  • LogP:2.49350 
Purity/Quality:

95%-98% *data from raw suppliers

Scabioside C *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of Scabioside C

There total 2 articles about Scabioside C 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:

Guidance literature:
Trihydrat C41H66O13*3H2O: aus Saponin IV, CH3OH /HCl;
DOI:10.1248/cpb.26.1666
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