Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

7-Triethylsilyl-13-oxobaccatin III

Base Information
  • Chemical Name:7-Triethylsilyl-13-oxobaccatin III
  • CAS No.:150665-56-8
  • Molecular Formula:C37H50O11Si
  • Molecular Weight:698.883
  • Hs Code.:
  • Mol file:150665-56-8.mol
7-Triethylsilyl-13-oxobaccatin III

Synonyms:7-O-triethylsilyl-13-keto baccatin III

Suppliers and Price of 7-Triethylsilyl-13-oxobaccatin III
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
  • TRC
  • 7-Triethylsilyl-13-oxobaccatinIII
  • 50mg
  • $ 1190.00
  • Medical Isotopes, Inc.
  • 7-Triethylsilyl-13-oxobaccatinIII
  • 5 mg
  • $ 650.00
Total 1 raw suppliers
Chemical Property of 7-Triethylsilyl-13-oxobaccatin III
Chemical Property:
  • Melting Point:212 °C 
  • Boiling Point:721.7±60.0 °C(Predicted) 
  • PKA:11.98±0.70(Predicted) 
  • Density:1.24±0.1 g/cm3(Predicted) 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly) 
Purity/Quality:

7-Triethylsilyl-13-oxobaccatinIII *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 7-Triethylsilyl-13-oxobaccatin III is used in the preparation of taxol analogs as antineoplastic agents and taxoids derivatives useful due to their ability to activate murine macrophages and inhibit the growth of macrophage-like cells. Baccatin III (B101000) derivative, used in the preparation of taxol analogs as antineoplastic agents and taxoids derivatives useful due to their ability to activate murine macrophages and inhibit the growth of macrophage-like cells.
Technology Process of 7-Triethylsilyl-13-oxobaccatin III

There total 14 articles about 7-Triethylsilyl-13-oxobaccatin III 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 dipyridinium dichromate; In dichloromethane; at 20 ℃; for 1.5h;
DOI:10.1039/c3ob40407b
Guidance literature:
With tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1021/jo011183q
Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 150665-56-8