Deoxyuridine triphosphate

Base Information

Chemical Name:Deoxyuridine triphosphate
CAS No.:1173-82-6
Molecular Formula:C₉H₁₅N₂O₁₄P₃
Molecular Weight:468.144
Hs Code.:
DSSTox Substance ID:DTXSID60908053
Nikkaji Number:J315.490D
Wikidata:Q28529690
NCI Thesaurus Code:C104002
Metabolomics Workbench ID:37652
ChEMBL ID:CHEMBL374361
Mol file:1173-82-6.mol

Synonyms:2'-deoxyuridine 5'-triphosphate;deoxy-UTP;deoxyuridine triphosphate

Suppliers and Price of Deoxyuridine triphosphate

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

American Custom Chemicals Corporation
((2R,3S,5R)-5-(2,4-DIOXO-3,4-DIHYDROPYRIMIDIN-1(2H)-YL)-3-HYDROXYTETRAHYDROFURAN-2-YL)METHYL TETRAHYDROGEN TRIPHOSPHATE 95.00%
5MG
$ 496.39

Total 15 raw suppliers

Chemical Property of Deoxyuridine triphosphate

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：273.57000
Density:2.01g/cm³
LogP:-1.47170
XLogP3:-5.5
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:14
Rotatable Bond Count:8
Exact Mass:467.97361415
Heavy Atom Count:28
Complexity:808

Purity/Quality:

98%,99%, ^*data from raw suppliers

((2R,3S,5R)-5-(2,4-DIOXO-3,4-DIHYDROPYRIMIDIN-1(2H)-YL)-3-HYDROXYTETRAHYDROFURAN-2-YL)METHYL TETRAHYDROGEN TRIPHOSPHATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Biological Agents -> Nucleic Acids and Derivatives
Canonical SMILES:C1C(C(OC1N2C=CC(=O)NC2=O)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O
Isomeric SMILES:C1[C@@H]([C@H](O[C@H]1N2C=CC(=O)NC2=O)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O

Technology Process of Deoxyuridine triphosphate

There total 8 articles about Deoxyuridine triphosphate 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: 12.0%

: C₉H₁₄N₂O₁₅P₄

: 1173-82-6,94234-60-3
2'-deoxyuridine-5'-triphosphate

Guidance literature:: With pyridine; water; iodine; In N,N-dimethyl-formamide; at 20 ℃; for 2.25h;

Reference yield:

: C₁₄H₂₂N₃O₇P

: 1173-82-6,94234-60-3
2'-deoxyuridine-5'-triphosphate

Guidance literature:: With tris(tetra-n-butylammonium) hydrogen pyrophosphate; In tetrahydrofuran; at 20 ℃; for 0.5h;
DOI:10.1021/ol049267j

Reference yield:

: (4-Chloro-butyl)-methyl-phosphoramidic acid benzyl ester (2R,3S,5R)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-hydroxy-tetrahydro-furan-2-ylmethyl ester

: 1173-82-6,94234-60-3
2'-deoxyuridine-5'-triphosphate

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Pd/C / tetrahydrofuran / 2 h / 20 °C

2: 52 mg / tris(tetra-n-butylammonium) hydrogen pyrophosphate / tetrahydrofuran / 0.5 h / 20 °C

With hydrogen; tris(tetra-n-butylammonium) hydrogen pyrophosphate; palladium on activated charcoal; In tetrahydrofuran;
DOI:10.1021/ol049267j