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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)-

6-bromo-4-iodoquinoline

Brc1ccc2c(c1)c(I)ccn2 Request for Quotation
Chemical Name: 6-bromo-4-iodoquinoline
CAS Number: 927801-23-8
Product Number: AG00GU07(AGN-PC-01LRAT)
Synonyms:
MDL No:
Molecular Formula: C9H5BrIN
Molecular Weight: 333.9512

Identification/Properties

Computed Properties
Molecular Weight:
333.954g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
332.865g/mol
Monoisotopic Mass:
332.865g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
165
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Bromo-4-iodoquinoline, a versatile intermediate in organic synthesis, plays a crucial role as a building block for creating novel compounds with unique properties and functionalities. This compound is commonly utilized in the development of pharmaceuticals, agrochemicals, and materials science due to its structural flexibility and reactivity. The presence of both bromine and iodine atoms in the quinoline ring enables selective modifications through various chemical reactions, such as substitution, addition, and cyclization processes. In particular, 6-Bromo-4-iodoquinoline serves as a valuable precursor for constructing biologically active molecules, heterocyclic scaffolds, and functional materials with tailored structures and properties. Its strategic placement of halogen substituents provides opportunities for fine-tuning the physicochemical characteristics and biological activities of the derived compounds, making it a critical component in modern synthetic chemistry and drug discovery efforts.