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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-chloro-3-iodopyridine-4-carbonitrile

N#Cc1ccnc(c1I)Cl Request for Quotation
Chemical Name: 2-chloro-3-iodopyridine-4-carbonitrile
CAS Number: 908279-56-1
Product Number: AG006A5N(AGN-PC-00HG80)
Synonyms:
MDL No:
Molecular Formula: C6H2ClIN2
Molecular Weight: 264.4510

Identification/Properties

Properties
Storage:
Light sensitive;Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
264.45g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
263.895g/mol
Monoisotopic Mass:
263.895g/mol
Topological Polar Surface Area:
36.7A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
164
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-3-iodoisonicotinonitrile is a key intermediate compound widely used in chemical synthesis for various applications. Due to its unique structural properties, this compound is particularly valuable in the field of organic chemistry as a versatile building block in the development of pharmaceuticals, agrochemicals, and advanced materials. The presence of both chlorine and iodine atoms in its structure enables 2-Chloro-3-iodoisonicotinonitrile to participate in a diverse range of chemical reactions, making it a valuable tool for custom synthesis of complex molecules. This compound is often employed as a precursor for the synthesis of pharmaceutical drugs, where its reactivity and selective functional groups play a crucial role in the formation of specific chemical bonds required for therapeutic activity. Additionally, 2-Chloro-3-iodoisonicotinonitrile finds application in the preparation of advanced materials such as polymers and specialty chemicals, where its strategic positioning of halogen substituents allows for controlled modification of molecular structures, leading to enhanced properties and performance. In summary, the utility of 2-Chloro-3-iodoisonicotinonitrile in chemical synthesis lies in its ability to serve as a versatile synthetic intermediate for the construction of complex molecules with tailored functionality and properties.