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(2'S, 3'R)-Cabazitaxel

Base Information Edit
  • Chemical Name:(2'S, 3'R)-Cabazitaxel
  • CAS No.:1714967-27-7
  • Molecular Formula:C45H57NO14
  • Molecular Weight:835.946
  • Hs Code.:
  • Mol file:1714967-27-7.mol
(2'S, 3'R)-Cabazitaxel

Synonyms:(2'S, 3'R)-Cabazitaxel

Suppliers and Price of (2'S, 3'R)-Cabazitaxel
Supply Marketing:Edit
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
  • TRC
  • (2’S,3’R)-Cabazitaxel(~90%)
  • 5mg
  • $ 690.00
  • A2B
  • (2’S,3’R)-Cabazitaxel
  • 10mg
  • $ 1338.00
  • A2B
  • (2’S,3’R)-Cabazitaxel
  • 5mg
  • $ 839.00
Total 3 raw suppliers
Chemical Property of (2'S, 3'R)-Cabazitaxel Edit
Chemical Property:
  • Boiling Point:870.7±65.0 °C(Predicted) 
  • PKA:11.20±0.46(Predicted) 
  • Density:1.31±0.1 g/cm3(Predicted) 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
Purity/Quality:

> 95% *data from raw suppliers

(2’S,3’R)-Cabazitaxel(~90%) *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses (2’S, 3’R)-Cabazitaxel is a stereoisomer of Cabazitaxel (C046500), a novel tubulin binding taxane, that acts as a second-line treatment for those with castration-resistant prostate cancer.
Technology Process of (2'S, 3'R)-Cabazitaxel

There total 73 articles about (2'S, 3'R)-Cabazitaxel 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 methanol; at 20 ℃; for 2h;
Guidance literature:
With hydrogenchloride; In tetrahydrofuran; ethanol; at -8 - 0 ℃; for 23.5h;
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