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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)-

2,3-dichloropyridine-4-carbaldehyde

O=Cc1ccnc(c1Cl)Cl Request for Quotation
Chemical Name: 2,3-dichloropyridine-4-carbaldehyde
CAS Number: 884495-41-4
Product Number: AG0036BF(AGN-PC-05ZTCQ)
Synonyms:
MDL No:
Molecular Formula: C6H3Cl2NO
Molecular Weight: 176.0001

Identification/Properties

Properties
MP:
94-96 °C
BP:
239.7°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
175.996g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
174.959g/mol
Monoisotopic Mass:
174.959g/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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 2,3-Dichloropyridine-4-carboxaldehyde is a key reagent in chemical synthesis, particularly in the production of pharmaceutical intermediates and agrochemicals. Its unique structure and properties make it a versatile building block in the creation of various functionalized molecules.2,3-Dichloropyridine-4-carboxaldehyde can be used as a starting material in the synthesis of heterocyclic compounds, such as pyridine derivatives, which are widely used in medicinal chemistry. It serves as a valuable intermediate for the preparation of active pharmaceutical ingredients (APIs) and biologically active molecules by undergoing various transformations, including nucleophilic substitution reactions and condensations.Furthermore, this compound plays a crucial role in the development of new pesticides and herbicides due to its ability to form complex structures with potent biological activities. Its presence in the chemical synthesis pathway enables the creation of novel chemical entities with enhanced pesticidal or herbicidal properties, contributing to the advancement of crop protection technologies.Overall, 2,3-Dichloropyridine-4-carboxaldehyde is a versatile and indispensable tool in chemical synthesis, offering diverse opportunities for the design and production of valuable compounds in the fields of pharmaceuticals and agrochemicals.