3-Bromo-4-methoxy-5-azaindole|1000341-22-9,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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-Bromo-4-methoxy-5-azaindole

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Chemical Name:	3-Bromo-4-methoxy-5-azaindole
CAS Number:	1000341-22-9
Product Number:	AG0000FR(AGN-PC-04Q64L)
Synonyms:
MDL No:
Molecular Formula:	C8H7BrN2O
Molecular Weight:	227.0580

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Chemical Structure

3-Bromo-4-methoxy-1H-pyrrolo[3,2-c]pyridine is a versatile compound used in chemical synthesis for its unique properties and functional groups. This compound serves as a key building block in the development of pharmaceuticals, agrochemicals, and electronic materials. With its bromine and methoxy substituents, 3-Bromo-4-methoxy-1H-pyrrolo[3,2-c]pyridine can undergo various reactions such as nucleophilic substitution, Suzuki coupling, and palladium-catalyzed cross-coupling reactions. This allows for the synthesis of complex molecules with tailored structures and properties, making it an essential tool in the field of organic chemistry.