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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, 4-chloro-3-nitro-

[O-][N+](=O)c1c(Cl)cc[nH]c1=O Request for Quotation
Chemical Name: 2(1H)-Pyridinone, 4-chloro-3-nitro-
CAS Number: 165547-79-5
Product Number: AG001W7P(AGN-PC-0JS8SC)
Synonyms:
MDL No:
Molecular Formula: C5H3ClN2O3
Molecular Weight: 174.5419

Identification/Properties

Properties
MP:
222-224 °C
BP:
283.4°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
174.54g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
173.983g/mol
Monoisotopic Mass:
173.983g/mol
Topological Polar Surface Area:
74.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
276
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


4-Chloro-2-hydroxy-3-nitropyridine is a versatile compound commonly used in chemical synthesis as a building block for pharmaceuticals, agrochemicals, and specialty chemicals. With its unique structure, this compound serves as a valuable intermediate in the production of various complex molecules.In chemical synthesis, 4-Chloro-2-hydroxy-3-nitropyridine acts as a key starting material for the synthesis of a wide range of compounds due to its ability to undergo various functional group transformations. This compound can participate in substitution reactions, cyclization reactions, and other transformations to yield products with diverse chemical structures and properties.The presence of a chloro, hydroxy, and nitro group on the pyridine ring of 4-Chloro-2-hydroxy-3-nitropyridine enables chemists to introduce additional functional groups or modify existing ones, allowing for the creation of novel molecules with desired properties. Its versatility and reactivity make it an essential component in the toolbox of synthetic chemists working in the pharmaceutical, agricultural, and specialty chemical industries.Overall, 4-Chloro-2-hydroxy-3-nitropyridine plays a vital role in chemical synthesis by enabling the efficient and controlled construction of complex molecules for various applications in the fields of medicine, agriculture, and materials science.