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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)-

2,5-Dibromopyridine-4-carboxaldehyde

O=Cc1cc(Br)ncc1Br Request for Quotation
Chemical Name: 2,5-Dibromopyridine-4-carboxaldehyde
CAS Number: 959244-28-1
Product Number: AG006A54(AGN-PC-056KY0)
Synonyms:
MDL No:
Molecular Formula: C6H3Br2NO
Molecular Weight: 264.9021

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
264.904g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
264.856g/mol
Monoisotopic Mass:
262.858g/mol
Topological Polar Surface Area:
30A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
131
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:
Danger
UN#:
2811
Hazard Statements:
H301
Precautionary Statements:
P301+P310
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,5-Dibromoisonicotinaldehyde is a versatile compound commonly employed in chemical synthesis as a key building block for the preparation of various organic molecules. Its unique structure and properties make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. In particular, this compound is often utilized in the production of heterocyclic compounds due to its ability to participate in numerous types of reactions, including condensation, alkylation, and substitution reactions.One of the important applications of 2,5-Dibromoisonicotinaldehyde in chemical synthesis is its role as a precursor for the synthesis of biologically active compounds. By selectively modifying the functional groups on the molecule, chemists can tailor the structure of the final product to exhibit specific pharmacological properties. This versatile compound has been utilized in the development of new drugs, including anti-cancer agents, antimicrobial agents, and anti-inflammatory drugs.Additionally, 2,5-Dibromoisonicotinaldehyde is widely used in the synthesis of fluorescent dyes and organic materials for electronic devices. Its unique fluorescent properties make it suitable for applications in the field of materials science, where it can be incorporated into polymers, conducting materials, and sensors. Furthermore, this compound can serve as a valuable precursor for the preparation of ligands and catalysts in coordination chemistry, enabling the synthesis of complex metal complexes with diverse applications in catalysis and materials science.Overall, 2,5-Dibromoisonicotinaldehyde plays a significant role in chemical synthesis by serving as a versatile building block for the construction of valuable molecules with diverse applications in pharmaceuticals, materials science, and catalysis. Its unique structural features and reactivity make it a valuable tool for chemists seeking to innovate and develop new compounds with tailored properties and functions.