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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)-

1H-Pyrrolo[2,3-b]pyridine, 4-chloro-2-iodo-1-[(4-methylphenyl)sulfonyl]-

Cc1ccc(cc1)S(=O)(=O)n1c(I)cc2c1nccc2Cl Request for Quotation
Chemical Name: 1H-Pyrrolo[2,3-b]pyridine, 4-chloro-2-iodo-1-[(4-methylphenyl)sulfonyl]-
CAS Number: 348640-26-6
Product Number: AG007H6E(AGN-PC-03RW3R)
Synonyms:
MDL No:
Molecular Formula: C14H10ClIN2O2S
Molecular Weight: 432.6639

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Tosyl-4-chloro-2-iodo-7-azaindole is a versatile compound that finds widespread application in chemical synthesis. Due to its unique structure and reactivity, this compound serves as a valuable building block in the creation of various organic molecules. In the realm of medicinal chemistry, N-Tosyl-4-chloro-2-iodo-7-azaindole is employed in the development of pharmaceuticals and bioactive compounds. Its incorporation in synthetic pathways enables the construction of complex molecular frameworks with precision. Furthermore, this compound is utilized in the synthesis of heterocyclic compounds, serving as a key intermediate in the production of diverse chemical entities. Its ability to participate in diverse chemical transformations makes it a valuable tool for synthetic chemists seeking to access novel compounds with specific functionalities. By leveraging the unique reactivity of N-Tosyl-4-chloro-2-iodo-7-azaindole, researchers can expedite the synthesis of target molecules and streamline the overall synthetic process.