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Cabazitaxel-d6

Base Information
  • Chemical Name:Cabazitaxel-d6
  • CAS No.:1383561-29-2
  • Molecular Formula:C45H57NO14
  • Molecular Weight:841.898
  • Hs Code.:
  • Mol file:1383561-29-2.mol
Cabazitaxel-d6

Synonyms:d6-cabazitaxel

Suppliers and Price of Cabazitaxel-d6
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
  • Cabazitaxel-d6
  • 1mg
  • $ 531.00
  • TRC
  • Cabazitaxel-d6(~90%)
  • 1mg
  • $ 245.00
  • Medical Isotopes, Inc.
  • Cabazitaxel-d6
  • 1 mg
  • $ 490.00
Total 11 raw suppliers
Chemical Property of Cabazitaxel-d6
Chemical Property:
  • Melting Point:151-158°C 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
Purity/Quality:

97% *data from raw suppliers

Cabazitaxel-d6 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Cabazitaxel-d6 is a labelled novel semi-synthetic taxane with antitumor activity used for the treatment of castration-resistant prostate cancer. A microtubule inhibitor. Cabazitaxel-d6 can be intended for use as an internal standard for the quantification of Cabazitaxel by GC- or LC-mass spectrometry.
Technology Process of Cabazitaxel-d6

There total 3 articles about Cabazitaxel-d6 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:
Guidance literature:
With hydrogenchloride; ethanol; at 0 ℃; Inert atmosphere;
Guidance literature:
Multi-step reaction with 2 steps
1: dmap; dicyclohexyl-carbodiimide / ethyl acetate / 20 °C / Molecular sieve; Inert atmosphere
2: hydrogenchloride; ethanol / 0 °C / Inert atmosphere
With hydrogenchloride; dmap; ethanol; dicyclohexyl-carbodiimide; In ethyl acetate;
Guidance literature:
Multi-step reaction with 3 steps
1: potassium hydride / tetrahydrofuran / 8 h / -20 - 20 °C
2: dmap; dicyclohexyl-carbodiimide / ethyl acetate / 20 °C / Molecular sieve; Inert atmosphere
3: hydrogenchloride; ethanol / 0 °C / Inert atmosphere
With hydrogenchloride; dmap; ethanol; potassium hydride; dicyclohexyl-carbodiimide; In tetrahydrofuran; ethyl acetate;
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