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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-chloro-3-iodo-1H-pyrrolo[2,3-c]pyridine

Clc1ncc2c(c1)c(I)c[nH]2 Request for Quotation
Chemical Name: 5-chloro-3-iodo-1H-pyrrolo[2,3-c]pyridine
CAS Number: 1190310-51-0
Product Number: AG000HFW(AGN-PC-09RUVN)
Synonyms:
MDL No:
Molecular Formula: C7H4ClIN2
Molecular Weight: 278.4775

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Chemical Structure


1H-Pyrrolo[2,3-c]pyridine, 5-chloro-3-iodo- is a valuable building block in chemical synthesis due to its unique structural properties and reactivity. This compound serves as a versatile intermediate in the preparation of various complex organic molecules. Its strategic placement of chlorine and iodine atoms enables diverse functional group transformations, allowing for efficient and selective derivatization. In organic synthesis, 1H-Pyrrolo[2,3-c]pyridine, 5-chloro-3-iodo- has been utilized in the construction of heterocyclic compounds, pharmaceuticals, agrochemicals, and materials with tailored properties. Its presence imparts specific steric and electronic effects that impact the overall reactivity and performance of the final products.