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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)-

2(1H)-Pyridinone, 5-chloro-3-iodo-

Clc1cc(I)c(=O)[nH]c1 Request for Quotation
Chemical Name: 2(1H)-Pyridinone, 5-chloro-3-iodo-
CAS Number: 188057-28-5
Product Number: AG002GNT(AGN-PC-02GQ0O)
Synonyms:
MDL No:
Molecular Formula: C5H3ClINO
Molecular Weight: 255.4409

Identification/Properties

Computed Properties
Molecular Weight:
255.439g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
254.895g/mol
Monoisotopic Mass:
254.895g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
209
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Chloro-3-iodopyridin-2(1H)-one is a versatile chemical compound that finds significant application in chemical synthesis processes. This compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure enables it to participate in a wide range of reactions, allowing for the creation of complex molecular structures efficiently.In organic synthesis, 5-Chloro-3-iodopyridin-2(1H)-one can be used as a precursor for the introduction of functional groups, such as halogens or heteroatoms, into organic molecules. It can also serve as a key intermediate in the preparation of biologically active compounds with potential therapeutic applications.Furthermore, this compound is often employed in transition metal-catalyzed cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds. These reactions enable chemists to construct complex molecular architectures with high precision and control over the stereochemistry.Overall, the strategic incorporation of 5-Chloro-3-iodopyridin-2(1H)-one in chemical synthesis processes offers chemists a powerful tool for the efficient and modular construction of diverse molecular scaffolds with tailored properties and functionalities.