1. Home
  2. 4-Pyridinecarboxamide, 2,6-dichloro-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

4-Pyridinecarboxamide, 2,6-dichloro-

NC(=O)c1cc(Cl)nc(c1)Cl Request for Quotation
Chemical Name: 4-Pyridinecarboxamide, 2,6-dichloro-
CAS Number: 89281-13-0
Product Number: AG0040R6(AGN-PC-0KL17W)
Synonyms:
MDL No:
Molecular Formula: C6H4Cl2N2O
Molecular Weight: 191.0148

Identification/Properties

Properties
MP:
202 °C
BP:
298.1 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
191.011g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
189.97g/mol
Monoisotopic Mass:
189.97g/mol
Topological Polar Surface Area:
56A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
155
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-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2,6-Dichloroisonicotinamide, also known as DCINA, is a valuable chemical reagent widely used in chemical synthesis processes. This compound plays a crucial role in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Specifically, it serves as a key building block in the production of biologically active compounds due to its unique structural properties.One important application of 2,6-Dichloroisonicotinamide in chemical synthesis is its involvement in the preparation of heterocyclic compounds. By utilizing DCINA as a starting material, chemists can efficiently synthesize diverse heterocycles such as pyridines, quinolines, and pyrimidines, which are essential structural motifs found in many bioactive molecules. This enables the creation of novel drug candidates, pesticides, and other functional materials with potential applications in various industries.Furthermore, 2,6-Dichloroisonicotinamide is commonly employed as a versatile intermediate in the production of complex organic compounds. Its ability to undergo selective chemical transformations, including substitution reactions and cross-coupling processes, makes it a valuable tool for modifying molecular structures and generating diverse chemical libraries. This versatility allows researchers to tailor the properties and functionalities of target molecules, leading to the discovery of new compounds with improved biological activity or environmental performance.In summary, 2,6-Dichloroisonicotinamide is a versatile compound with significant utility in chemical synthesis, particularly for the construction of heterocyclic compounds and complex organic molecules. Its role as a key building block enables the efficient preparation of diverse chemical entities with potential applications in drug discovery, agriculture, and materials science.