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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)-

5-bromo-2-fluoro-3-nitropyridine

Brc1cnc(c(c1)[N+](=O)[O-])F Request for Quotation
Chemical Name: 5-bromo-2-fluoro-3-nitropyridine
CAS Number: 886372-98-1
Product Number: AG0036AG(AGN-PC-05IUBF)
Synonyms:
MDL No:
Molecular Formula: C5H2BrFN2O2
Molecular Weight: 220.9840

Identification/Properties

Properties
BP:
272.8 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
220.985g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
219.928g/mol
Monoisotopic Mass:
219.928g/mol
Topological Polar Surface Area:
58.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
163
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-Bromo-2-fluoro-3-nitropyridine is a versatile chemical compound widely utilized in chemical synthesis due to its unique properties and reactivity. This compound is commonly employed as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and advanced materials. Its strategic incorporation in organic reactions can lead to the formation of novel molecular structures with diverse functionalities and applications.One important application of 5-Bromo-2-fluoro-3-nitropyridine is in the development of complex organic molecules through coupling reactions such as Suzuki, Heck, and Sonogashira reactions. By serving as a precursor, this compound enables the introduction of specific functional groups or substitution patterns into target molecules, allowing chemists to tailor the properties of the final product for specific purposes. Additionally, the presence of both bromine and fluoro substituents in the pyridine ring enhances its reactivity and compatibility with a wide range of synthetic protocols.Furthermore, 5-Bromo-2-fluoro-3-nitropyridine can also be utilized as a valuable intermediate in the synthesis of heterocyclic compounds, which are essential structural motifs in many bioactive molecules. Its ability to participate in regioselective transformations and form strong bonds with various nucleophiles makes it a valuable tool for constructing complex molecular architectures. Overall, the versatility and synthetic utility of 5-Bromo-2-fluoro-3-nitropyridine make it a valuable asset in modern organic chemistry research and drug discovery efforts.