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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)-

4-iodopyrimidin-5-amine

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Chemical Name: 4-iodopyrimidin-5-amine
CAS Number: 942067-98-3
Product Number: AG00H142(AGN-PC-0JF433)
Synonyms:
MDL No:
Molecular Formula: C4H4IN3
Molecular Weight: 220.9991

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Iodopyrimidin-5-amine, also known as $name$, is a versatile chemical compound commonly used in chemical synthesis processes. This compound plays a crucial role in the development of various pharmaceuticals, agrochemicals, and materials due to its unique reactivity and functional group properties.In chemical synthesis, 4-Iodopyrimidin-5-amine serves as a key building block for the construction of heterocyclic compounds. Its iodine substituent and amine group make it a valuable reagent for introducing functional groups in complex molecule synthesis. This compound is often employed in cross-coupling reactions, nucleophilic substitutions, and other transformations to facilitate the creation of novel organic molecules.Furthermore, 4-Iodopyrimidin-5-amine is utilized in the preparation of biologically active compounds, such as antiviral agents, kinase inhibitors, and fluorescent dyes. Its structural features enable the modification of specific regions within a molecule, leading to enhanced biological activity and selectivity in drug discovery research.Overall, the application of 4-Iodopyrimidin-5-amine in chemical synthesis enables chemists to access diverse chemical space and design innovative compounds with potential therapeutic or industrial applications.