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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, 5-iodo-

OC[C@H]1O[C@H]([C@@H]([C@@H]1O)O)n1cc(I)c(=O)[nH]c1=O Request for Quotation
Chemical Name: Uridine, 5-iodo-
CAS Number: 1024-99-3
Product Number: AG0007DA(AGN-PC-0NVEXJ)
Synonyms:
MDL No:
Molecular Formula: C9H11IN2O6
Molecular Weight: 370.0979

Identification/Properties

Computed Properties
Molecular Weight:
370.099g/mol
XLogP3:
-1.3
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
369.966g/mol
Monoisotopic Mass:
369.966g/mol
Topological Polar Surface Area:
119A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
414
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Iodouridine is a versatile chemical compound that plays a crucial role in chemical synthesis. As a modified nucleoside, it is commonly utilized in the development of nucleotide analogs and pharmaceutical compounds. In particular, 5-Iodouridine is often employed in the synthesis of antiviral and anticancer drugs due to its ability to interfere with nucleic acid replication processes. Additionally, this compound is a valuable tool in the study of RNA structures and functions, making it a key component in biochemical research and drug discovery efforts. Its unique properties and diverse applications in chemical synthesis highlight the significance of 5-Iodouridine in advancing the fields of chemistry and medicine.