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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)-

Quinoline, 7-chloro-4-iodo-

Clc1ccc2c(c1)nccc2I Request for Quotation
Chemical Name: Quinoline, 7-chloro-4-iodo-
CAS Number: 98591-57-2
Product Number: AG003NEJ(AGN-PC-0NHAS4)
Synonyms:
MDL No:
Molecular Formula: C9H5ClIN
Molecular Weight: 289.5002

Identification/Properties

Properties
MP:
125-129 °C(lit.)
Storage:
2-8℃;Light sensitive;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Chloro-4-iodoquinoline is a versatile chemical compound that finds valuable applications in chemical synthesis processes. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique reactivity and structural properties. In chemical synthesis, 7-Chloro-4-iodoquinoline can be utilized as a precursor in the production of complex organic molecules through functional group transformations, such as nucleophilic substitution and palladium-catalyzed coupling reactions. Its halogen substituents enable selective functionalization at specific positions, allowing for the creation of a diverse range of derivative compounds with tailored properties. Additionally, the quinoline core of this molecule imparts desirable aromatic and heterocyclic characteristics, making it highly desirable for the construction of biologically active compounds and advanced materials.