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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)-

4,6-dibromo-2-nitropyridin-3-ol

Brc1cc(Br)c(c(n1)[N+](=O)[O-])O Request for Quotation
Chemical Name: 4,6-dibromo-2-nitropyridin-3-ol
CAS Number: 916737-75-2
Product Number: AG00IGU0(AGN-PC-0BWDYW)
Synonyms:
MDL No:
Molecular Formula: C5H2Br2N2O3
Molecular Weight: 297.8890

Identification/Properties

Computed Properties
Molecular Weight:
297.89g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
297.841g/mol
Monoisotopic Mass:
295.843g/mol
Topological Polar Surface Area:
78.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
186
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,6-Dibromo-2-nitropyridin-3-ol is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. One of its key applications is as a building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. This compound serves as a valuable intermediate in the production of specialized organic molecules due to its ability to undergo selective chemical transformations such as reduction, halogenation, and substitution reactions. Additionally, 4,6-Dibromo-2-nitropyridin-3-ol can be utilized in the preparation of complex heterocyclic compounds through cyclization reactions, making it a valuable tool in the field of medicinal chemistry and drug discovery. Its strategic placement of bromine and nitro groups on the pyridine ring allows for controlled functional group manipulation, enabling chemists to tailor the structure of organic molecules for specific applications. By incorporating 4,6-Dibromo-2-nitropyridin-3-ol into synthetic pathways, researchers can access a diverse array of chemical compounds with potential pharmacological, agricultural, or material science relevance.