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7,13-Bis-O-(triethylsilyl)-10-deacetyl-10-oxo Baccatin III

Base Information
  • Chemical Name:7,13-Bis-O-(triethylsilyl)-10-deacetyl-10-oxo Baccatin III
  • CAS No.:651293-82-2
  • Molecular Formula:C41H62O10Si2
  • Molecular Weight:771.108
  • Hs Code.:
  • Mol file:651293-82-2.mol
7,13-Bis-O-(triethylsilyl)-10-deacetyl-10-oxo Baccatin III

Synonyms:7,13-bis(triethylsilyl)-10-dehydro-10-deacetylbaccatin III

Suppliers and Price of 7,13-Bis-O-(triethylsilyl)-10-deacetyl-10-oxo Baccatin 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
  • 7,13-Bis-O-(triethylsilyl)-10-deacetyl-10-oxoBaccatinIII
  • 2.5mg
  • $ 275.00
  • Medical Isotopes, Inc.
  • 7,13-Bis-O-(triethylsilyl)-10-deacetyl-10-oxoBaccatinIII
  • 25 mg
  • $ 3000.00
  • Medical Isotopes, Inc.
  • 7,13-Bis-O-(triethylsilyl)-10-deacetyl-10-oxoBaccatinIII
  • 2.5 mg
  • $ 750.00
Total 1 raw suppliers
Chemical Property of 7,13-Bis-O-(triethylsilyl)-10-deacetyl-10-oxo Baccatin III
Chemical Property:
  • Storage Temp.:Refrigerator 
  • Solubility.:Chloroform, Dichloromethane, Ethyl Acetate, Methanol 
Purity/Quality:

7,13-Bis-O-(triethylsilyl)-10-deacetyl-10-oxoBaccatinIII *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 10-Deacetylbaccatin III (D198250) derivative, 7,13-Bis-O-(triethylsilyl)-10-deacetyl-10-oxo Baccatin III is used in the preparation of taxane derivatives with antitumoral and antineoplastic properties.
Technology Process of 7,13-Bis-O-(triethylsilyl)-10-deacetyl-10-oxo Baccatin III

There total 2 articles about 7,13-Bis-O-(triethylsilyl)-10-deacetyl-10-oxo Baccatin 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:
10-dehydro 10-deacetyl 7-epibaccatin V; With pyridine; In ethyl acetate; toluene; at -20 - 40 ℃; for 1h;
triethylsilyl trifluoromethyl sulfonate; In ethyl acetate; toluene; at -10 - -5.8 ℃; for 2h;
Guidance literature:
Multi-step reaction with 2 steps
1: 75 percent / Cu(OAc)2*H2O; air / methanol / 72 h
2: 3 percent / imidazole / CH2Cl2 / 20 °C
With 1H-imidazole; copper diacetate; air; In methanol; dichloromethane;
DOI:10.1002/ejoc.200300376
Guidance literature:
7,13-bis(triethylsilyl)-10-dehydro-10-deacetylbaccatin III; With lithium borohydride; ethanol; In tetrahydrofuran; at -13.9 - 23 ℃;
With ammonium acetate; acetic acid; In tetrahydrofuran; ethanol; at 2.5 ℃; Product distribution / selectivity;
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