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

Encyclopedia

N-Trifluoroacetyladriamycin

Base Information Edit
  • Chemical Name:N-Trifluoroacetyladriamycin
  • CAS No.:26295-56-7
  • Molecular Formula:C29H28 F3 N O12
  • Molecular Weight:639.536
  • Hs Code.:
  • UNII:ITA96UBK4T
  • DSSTox Substance ID:DTXSID10949158
  • Nikkaji Number:J85.474C
  • Wikidata:Q27280887
  • Mol file:26295-56-7.mol
N-Trifluoroacetyladriamycin

Synonyms:AD 41;N-trifluoroacetyladriamycin

Suppliers and Price of N-Trifluoroacetyladriamycin
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
  • Usbiological
  • N-Trifluoroacetyldoxorubicin
  • 2mg
  • $ 446.00
  • Usbiological
  • N-Trifluoroacetyldoxorubicin
  • 5mg
  • $ 446.00
  • TRC
  • N-TrifluoroacetylDoxorubicin
  • 2mg
  • $ 70.00
  • Medical Isotopes, Inc.
  • N-Trifluoroacetyldoxorubicin
  • 50 mg
  • $ 2120.00
  • Medical Isotopes, Inc.
  • N-Trifluoroacetyldoxorubicin
  • 5 mg
  • $ 640.00
  • American Custom Chemicals Corporation
  • N-TRIFLUOROACETYLADRIAMYCIN 95.00%
  • 5MG
  • $ 502.29
Total 10 raw suppliers
Chemical Property of N-Trifluoroacetyladriamycin Edit
Chemical Property:
  • Vapor Pressure:3.7E-31mmHg at 25°C 
  • Melting Point:>150°C (dec.) 
  • Boiling Point:855.4°C at 760 mmHg 
  • PKA:7.35±0.60(Predicted) 
  • Flash Point:471.1°C 
  • PSA:209.15000 
  • Density:1.66g/cm3 
  • LogP:1.11200 
  • Solubility.:DMSO, Methanol 
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:6
  • Hydrogen Bond Acceptor Count:15
  • Rotatable Bond Count:6
  • Exact Mass:639.15635981
  • Heavy Atom Count:45
  • Complexity:1190
Purity/Quality:

99% *data from raw suppliers

N-Trifluoroacetyldoxorubicin *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1C(C(CC(O1)OC2CC(CC3=C2C(=C4C(=C3O)C(=O)C5=C(C4=O)C(=CC=C5)OC)O)(C(=O)CO)O)NC(=O)C(F)(F)F)O
  • Isomeric SMILES:C[C@H]1[C@H]([C@H](C[C@@H](O1)O[C@H]2C[C@@](CC3=C2C(=C4C(=C3O)C(=O)C5=C(C4=O)C(=CC=C5)OC)O)(C(=O)CO)O)NC(=O)C(F)(F)F)O
  • Uses Doxorubicin (D558000) metabolite. Cytotoxic interaction with DNA.
Technology Process of N-Trifluoroacetyladriamycin

There total 6 articles about N-Trifluoroacetyladriamycin 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 pyridine; In diethyl ether; at -30 - 0 ℃; for 3h; Schlenk technique;
Guidance literature:
With sodium methylate; In methanol; chloroform; at 23 ℃; for 22h;
DOI:10.1021/jm00138a005
Guidance literature:
With S-ethyltrifluoroacetate;
DOI:10.1080/00397919108019778
Post RFQ for Price