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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-FLUORO-3-IODO-1H-PYRROLO[2,3-B]PYRIDINE

Fc1cnc2c(c1)c(I)c[nH]2 Request for Quotation
Chemical Name: 5-FLUORO-3-IODO-1H-PYRROLO[2,3-B]PYRIDINE
CAS Number: 900514-10-5
Product Number: AG00GSUU(AGN-PC-04G0GD)
Synonyms:
MDL No:
Molecular Formula: C7H4FIN2
Molecular Weight: 262.0229

Identification/Properties

Properties
Storage:
Light sensitive;Keep in dry area;2-8℃;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Fluoro-3-iodo-1H-pyrrolo[2,3-b]pyridine is a versatile chemical compound commonly used in various chemical synthesis applications. This particular compound is valued for its ability to serve as a building block or substrate in organic synthesis processes.One important application of 5-Fluoro-3-iodo-1H-pyrrolo[2,3-b]pyridine is its use in the synthesis of pharmaceutical compounds. Its unique structure and reactivity make it a valuable intermediate in the preparation of bioactive molecules and drug candidates. By incorporating this compound into multi-step synthesis routes, chemists can access diverse chemical space and potentially discover new therapeutic agents.Additionally, 5-Fluoro-3-iodo-1H-pyrrolo[2,3-b]pyridine can also be employed in the development of agrochemicals, dyes, and materials. Its structural features enable it to participate in various coupling reactions, functional group transformations, and heterocycle formations, leading to the creation of novel compounds with tailored properties.Overall, the versatility and reactivity of 5-Fluoro-3-iodo-1H-pyrrolo[2,3-b]pyridine make it a valuable tool in the toolkit of synthetic chemists working in the fields of drug discovery, material science, and agrochemical development.