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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)-

5-bromo-4-chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine

Brc1cnc2c(c1Cl)c(I)c[nH]2 Request for Quotation
Chemical Name: 5-bromo-4-chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine
CAS Number: 1092579-75-3
Product Number: AG008Z19(AGN-PC-0BL83W)
Synonyms:
MDL No:
Molecular Formula: C7H3BrClIN2
Molecular Weight: 357.3736

Identification/Properties

Computed Properties
Molecular Weight:
357.373g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
355.821g/mol
Monoisotopic Mass:
355.821g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
183
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


5-Bromo-4-chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine is a valuable building block in chemical synthesis due to its unique structural properties. This compound serves as a versatile intermediate in the creation of pharmaceuticals, agrochemicals, and materials science applications. Its functional groups, specifically the bromine, chlorine, and iodine substituents, offer a wide range of reactivity for diverse synthetic pathways. In organic synthesis, this compound can participate in various reactions such as Suzuki coupling, Sonogashira coupling, and Buchwald-Hartwig amination, enabling the formation of complex molecular structures. The presence of multiple halogen atoms in 5-Bromo-4-chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine also facilitates further functionalization through cross-coupling reactions, making it a valuable tool for chemical modification and diversification. This compound's versatility and reactivity make it a crucial component in the development of novel compounds with potential applications in medicinal chemistry, material science, and other advanced fields.