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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, 3,5-dibromo-

Brc1cnc(c(c1)Br)O Request for Quotation
Chemical Name: 2(1H)-Pyridinone, 3,5-dibromo-
CAS Number: 13472-81-6
Product Number: AG0037TY(AGN-PC-0JU8BD)
Synonyms:
MDL No: MFCD00023472
Molecular Formula: C5H3Br2NO
Molecular Weight: 252.8914

Identification/Properties

Computed Properties
Molecular Weight:
252.893g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
252.856g/mol
Monoisotopic Mass:
250.858g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
207
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


The compound 3,5-Dibromo-2(1H)-Pyridinone is a versatile building block in chemical synthesis due to its unique chemical properties. It is commonly used as a reagent in organic synthesis reactions, particularly in the modification of heterocyclic compounds. This compound serves as an effective halogenating agent, facilitating the introduction of bromine atoms into organic molecules. Additionally, 3,5-Dibromo-2(1H)-Pyridinone is employed in the development of pharmaceuticals and agrochemicals, where its specific structural characteristics play a key role in enhancing the biological activity of the final products. In the field of materials science, this compound is utilized in the design of novel polymers and advanced materials, demonstrating its significance across various branches of chemistry.