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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, 6-iodo-8-nitro-

Ic1cc2cccnc2c(c1)[N+](=O)[O-] Request for Quotation
Chemical Name: Quinoline, 6-iodo-8-nitro-
CAS Number: 5552-46-5
Product Number: AG00DL58(AGN-PC-0NHKDC)
Synonyms:
MDL No:
Molecular Formula: C9H5IN2O2
Molecular Weight: 300.05267

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
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


6-Iodo-8-nitroquinoline is a versatile compound commonly utilized in chemical synthesis due to its various applications. This compound is frequently employed as a building block in the development of pharmaceuticals, agrochemicals, and materials science. Its unique structure and reactivity make it a valuable tool for organic chemists seeking to design and produce novel compounds with specific properties and functions. In particular, 6-Iodo-8-nitroquinoline is known for its ability to participate in various types of chemical reactions, including nucleophilic substitution, electrophilic aromatic substitution, and metal-catalyzed cross-coupling reactions. Its versatility and compatibility with a wide range of functional groups make it a valuable intermediate in the synthesis of complex organic molecules with diverse applications in the fields of medicinal chemistry, materials science, and chemical biology.