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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)-

2,4-dibromo-3-nitropyridine

[O-][N+](=O)c1c(Br)ccnc1Br Request for Quotation
Chemical Name: 2,4-dibromo-3-nitropyridine
CAS Number: 121263-10-3
Product Number: AG003FPJ(AGN-PC-03NRI5)
Synonyms:
MDL No: MFCD09750299
Molecular Formula: C5H2Br2N2O2
Molecular Weight: 281.8896

Identification/Properties

Properties
BP:
262.1°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
281.891g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
281.846g/mol
Monoisotopic Mass:
279.848g/mol
Topological Polar Surface Area:
58.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
161
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,4-Dibromo-3-nitropyridine is a versatile compound commonly used in chemical synthesis. Its primary application lies in its role as a building block in the creation of various pharmaceuticals, agrochemicals, and materials.In organic synthesis, 2,4-Dibromo-3-nitropyridine serves as a valuable intermediate due to its reactive nitro and bromo groups. These functional groups enable the compound to participate in a range of important reactions, including Suzuki couplings, nucleophilic substitutions, and palladium-catalyzed cross-couplings.The unique structure of 2,4-Dibromo-3-nitropyridine lends itself well to the modification and functionalization of molecules, allowing chemists to tailor its reactivity for specific synthetic pathways. Its presence in the synthesis of complex molecules highlights its significance in the field of medicinal chemistry and the development of innovative materials.