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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-Quinolinecarbonitrile, 4-chloro-7-iodo-

N#Cc1cnc2c(c1Cl)ccc(c2)I Request for Quotation
Chemical Name: 3-Quinolinecarbonitrile, 4-chloro-7-iodo-
CAS Number: 364793-64-6
Product Number: AG00C6DI(AGN-PC-0436U0)
Synonyms:
MDL No:
Molecular Formula: C10H4ClIN2
Molecular Weight: 314.5096

Identification/Properties

Properties
BP:
423.345°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-7-iodoquinoline-3-carbonitrile, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique structure and properties. This compound serves as an important building block in the development of various pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, 4-Chloro-7-iodoquinoline-3-carbonitrile acts as a key intermediate in the preparation of diverse organic molecules. Its functional groups and reactivity make it a valuable component in the synthesis of heterocyclic compounds, which are essential in drug discovery and development. Additionally, the presence of both chlorine and iodine atoms in the molecule provides opportunities for further derivatization, allowing researchers to tailor the compound for specific applications.Furthermore, the presence of the quinoline ring system in 4-Chloro-7-iodoquinoline-3-carbonitrile imparts certain pharmacological properties to the molecules it is incorporated into. This makes it a valuable starting material for the synthesis of bioactive compounds with potential therapeutic effects.Overall, the use of 4-Chloro-7-iodoquinoline-3-carbonitrile in chemical synthesis offers a versatile and efficient route to access complex molecules with diverse applications in the fields of medicine, agriculture, and materials science.