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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Uridine, 2'-deoxy-5-ethyl-

OC[C@H]1O[C@H](C[C@@H]1O)n1cc(CC)c(=O)[nH]c1=O Request for Quotation
Chemical Name: Uridine, 2'-deoxy-5-ethyl-
CAS Number: 15176-29-1
Product Number: AG00AOPE(AGN-PC-0O4BL7)
Synonyms:
MDL No:
Molecular Formula: C11H16N2O5
Molecular Weight: 256.2551

Identification/Properties

Computed Properties
Molecular Weight:
256.258g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
256.106g/mol
Monoisotopic Mass:
256.106g/mol
Topological Polar Surface Area:
99.1A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
395
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Edoxudine, also known as 5-iodo-2'-deoxyuridine, is a nucleoside analog that has found significant applications in chemical synthesis, particularly in the field of nucleoside chemistry. The unique properties of edoxudine make it a valuable building block for the synthesis of nucleoside analogs and related compounds.One key application of edoxudine in chemical synthesis is its use as a precursor in the synthesis of modified nucleosides. By leveraging the iodine moiety present in edoxudine, chemists can introduce various functional groups or modify the structure to create novel nucleoside analogs with desired properties. These analogs can be further utilized in pharmaceutical research and drug development.Additionally, edoxudine can serve as a versatile starting material for the preparation of radiolabeled nucleosides. The iodine-iodine exchange reaction of edoxudine enables the incorporation of radioactive iodine isotopes, facilitating the synthesis of radiolabeled nucleosides for use in biochemical assays, imaging studies, and nucleoside metabolism research.Overall, the application of edoxudine in chemical synthesis offers a wide range of possibilities for creating diverse nucleoside analogs and derivatives, showcasing its importance in the advancement of nucleoside chemistry and drug discovery efforts.