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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)-

Pyridine, 2-bromo-6-chloro-3-nitro-

[O-][N+](=O)c1ccc(nc1Br)Cl Request for Quotation
Chemical Name: Pyridine, 2-bromo-6-chloro-3-nitro-
CAS Number: 91678-23-8
Product Number: AG00GUII(AGN-PC-00LO99)
Synonyms:
MDL No:
Molecular Formula: C5H2BrClN2O2
Molecular Weight: 237.4386

Identification/Properties

Properties
BP:
277.2°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
237.437g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
235.899g/mol
Monoisotopic Mass:
235.899g/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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-6-chloro-3-nitropyridine is a versatile compound commonly used in chemical synthesis as a valuable building block for the preparation of various advanced organic molecules. This heterocyclic derivative possesses a unique structure that offers a wide range of applications in pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, 2-Bromo-6-chloro-3-nitropyridine plays a crucial role as a key intermediate in the production of complex organic compounds. Its functional groups enable it to participate in various reactions such as nucleophilic substitution, transition metal-catalyzed coupling, and palladium-catalyzed cross-coupling reactions. The presence of bromine, chlorine, and nitro groups in its structure provides opportunities for further functionalization to tailor its properties for specific synthetic goals.One of the notable applications of 2-Bromo-6-chloro-3-nitropyridine is in the synthesis of pharmaceutical agents, where it serves as a precursor to biologically active molecules with therapeutic potential. By incorporating this compound into the molecular structure of drug candidates, chemists can modulate their pharmacological properties, enhance specificity, and improve efficacy. Additionally, its use in agrochemical synthesis allows for the development of crop protection agents with enhanced activity and selectivity.Furthermore, in materials science, 2-Bromo-6-chloro-3-nitropyridine can be employed for the construction of functional materials and polymers with tailored properties. Its ability to participate in polymerization reactions enables the synthesis of advanced polymeric materials used in coatings, adhesives, and electronic devices. By leveraging the unique reactivity of this compound, researchers can design innovative materials with specific functionalities for diverse applications.Overall, the versatility of 2-Bromo-6-chloro-3-nitropyridine in chemical synthesis makes it a valuable tool for designing and accessing complex molecules with potential applications across various industries. Its strategic placement within synthetic pathways allows for efficient and targeted construction of intricate structures, highlighting its significance in advancing the field of organic chemistry.