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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-bromo-4-hydroxy-

Oc1cc[nH]c(=O)c1Br Request for Quotation
Chemical Name: 2(1H)-Pyridinone, 3-bromo-4-hydroxy-
CAS Number: 96245-97-5
Product Number: AG005VBQ(AGN-PC-0ABPGC)
Synonyms:
MDL No:
Molecular Formula: C5H4BrNO2
Molecular Weight: 189.9948

Identification/Properties

Properties
MP:
263.5-264.5℃ (decomp)
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
189.996g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
188.943g/mol
Monoisotopic Mass:
188.943g/mol
Topological Polar Surface Area:
49.3A^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


3-Bromo-4-hydroxypyridin-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 creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structure, it acts as a precursor in the synthesis of complex organic molecules by facilitating key reactions such as nucleophilic substitution and cross-coupling reactions.One important application of 3-Bromo-4-hydroxypyridin-2(1H)-one is its use as a starting material for the synthesis of heterocyclic compounds. These heterocycles are essential in drug discovery and development, as they often exhibit diverse biological activities. By incorporating 3-Bromo-4-hydroxypyridin-2(1H)-one into the synthesis pathway, chemists can access a wide range of structurally diverse molecules with potential pharmacological properties.Additionally, 3-Bromo-4-hydroxypyridin-2(1H)-one can be utilized in the preparation of chiral intermediates. Chirality plays a crucial role in modern drug design, as enantiopure compounds often exhibit different pharmacological profiles. Through appropriate functionalization and manipulation of the bromo-hydroxypyridinone scaffold, chemists can access chiral building blocks that are vital for the development of enantiomerically pure drug candidates.Overall, the strategic incorporation of 3-Bromo-4-hydroxypyridin-2(1H)-one in chemical synthesis enables chemists to access diverse chemical space, facilitating the creation of new and potentially bioactive molecules with important applications in various industries.