5'-O-Palmitoyl-5-fluoro-2'-deoxyuridine

Base Information

Chemical Name:5'-O-Palmitoyl-5-fluoro-2'-deoxyuridine
CAS No.:96733-83-4
Molecular Formula:C₂₅H₄₁FN₂O₆
Molecular Weight:484.609
Hs Code.:
DSSTox Substance ID:DTXSID10242474
Wikidata:Q83126199
Mol file:96733-83-4.mol

Synonyms:5'-O-palmitoyl-5-fluoro-2'-deoxyuridine;5-palmitoyl-FUDR

Suppliers and Price of 5'-O-Palmitoyl-5-fluoro-2'-deoxyuridine

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

Total 3 raw suppliers

Chemical Property of 5'-O-Palmitoyl-5-fluoro-2'-deoxyuridine

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：110.62000
Density:1.16g/cm³
LogP:4.34860
XLogP3:6.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:18
Exact Mass:484.29486519
Heavy Atom Count:34
Complexity:686

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCCCCCCCCCCC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)F)O
Isomeric SMILES:CCCCCCCCCCCCCCCC(=O)OC[C@@H]1[C@H](C[C@@H](O1)N2C=C(C(=O)NC2=O)F)O

Technology Process of 5'-O-Palmitoyl-5-fluoro-2'-deoxyuridine

There total 1 articles about 5'-O-Palmitoyl-5-fluoro-2'-deoxyuridine 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:

Reference yield:

: 693-38-9
vinyl palmitate

: 50-91-9
5-Fluoro-2'-deoxyuridine

: 96733-83-4
5'-O-palmitoyl-floxuridine

: 96733-84-5
3'-O-palmitoyl-floxuridine

: 7207-68-3
3',5'-di-O-palmitoyl-FUdR

Guidance literature:: With PSL-C; 1-n-butyl-2,3-dimethylimidazolium hexafluorophosphate; In tetrahydrofuran; at 50 ℃; regioselective reaction;
DOI:10.1016/j.tet.2008.11.045