3-iodo-4-methoxy-1H-pyrrolo[3,2-c]pyridine|1000341-25-2,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-iodo-4-methoxy-1H-pyrrolo[3,2-c]pyridine

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Chemical Name:	3-iodo-4-methoxy-1H-pyrrolo[3,2-c]pyridine
CAS Number:	1000341-25-2
Product Number:	AG0000FO(AGN-PC-04Q64M)
Synonyms:
MDL No:
Molecular Formula:	C8H7IN2O
Molecular Weight:	274.0585

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Identification/Properties

Safety Information

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N/A

Hazard Statements:

H302

Precautionary Statements:

P280-P305+P351+P338

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Chemical Structure

3-Iodo-4-methoxy-1H-pyrrolo[3,2-c]pyridine, commonly known as $name$, serves as a versatile building block in chemical synthesis due to its unique structural properties and reactivity. This compound finds extensive application in the development of pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, $name$ acts as a key intermediate in the creation of various heterocyclic compounds through functional group manipulation and strategic bond formation. Its characteristic iodo and methoxy substituents impart distinct reactivity, allowing for selective cross-coupling reactions and further derivatization to access diverse molecular scaffolds.Moreover, the presence of the pyrrolopyridine core in $name$ confers valuable aromaticity and conjugation, making it a desirable motif for constructing bioactive molecules and molecular probes with enhanced stability and activity. This compound's strategic placement of functional groups enables chemists to design efficient synthetic routes towards complex molecules with specific biological or material properties.Additionally, the reactivity and structural features of 3-Iodo-4-methoxy-1H-pyrrolo[3,2-c]pyridine make it a valuable tool in medicinal chemistry for the synthesis of potential drug candidates targeting various diseases and disorders. Its presence in molecular libraries allows for the rapid exploration of structure-activity relationships and the identification of lead compounds for further optimization.Overall, the versatile nature and synthetic utility of $name$ make it a valuable resource for chemical synthesis, enabling researchers to access novel compounds and accelerate the discovery of new materials and therapeutics.