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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)-

3-Pyridinecarboxaldehyde, 5-bromo-2-chloro-

O=Cc1cc(Br)cnc1Cl Request for Quotation
Chemical Name: 3-Pyridinecarboxaldehyde, 5-bromo-2-chloro-
CAS Number: 228251-24-9
Product Number: AG00365F(AGN-PC-03YOBI)
Synonyms:
MDL No:
Molecular Formula: C6H3BrClNO
Molecular Weight: 220.4511

Identification/Properties

Properties
BP:
278°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
220.45g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
218.909g/mol
Monoisotopic Mass:
218.909g/mol
Topological Polar Surface Area:
30A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
133
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-chloro-3-pyridinecarboxaldehyde is a versatile chemical reagent commonly used in organic synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique reactivity and functional groups. In chemical synthesis, 5-Bromo-2-chloro-3-pyridinecarboxaldehyde is frequently employed as a precursor in the synthesis of complex molecules through various synthetic routes.One important application of 5-Bromo-2-chloro-3-pyridinecarboxaldehyde is in the construction of heterocyclic compounds, specifically pyridine derivatives. By using this compound as a starting material, chemists can perform a range of reactions such as cross-coupling, nucleophilic addition, and condensation to introduce different functional groups onto the pyridine ring. This enables the synthesis of novel molecules with diverse pharmacological activities or other desired properties.Furthermore, 5-Bromo-2-chloro-3-pyridinecarboxaldehyde can participate in multi-step reactions to form more complex scaffolds, making it an essential intermediate in the synthesis of biologically active compounds. Its unique structural features allow for strategic modifications that can lead to the development of potential drug candidates or advanced materials for various applications. By leveraging the reactivity and versatility of this compound in chemical transformations, researchers can access a wide range of structurally diverse molecules with tailored properties.