6-fluoro-4-phenylmethoxy-1H-indole|312314-26-4,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)-

6-fluoro-4-phenylmethoxy-1H-indole

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Chemical Name:	6-fluoro-4-phenylmethoxy-1H-indole
CAS Number:	312314-26-4
Product Number:	AG00BJ7H(AGN-PC-0N7HGQ)
Synonyms:
MDL No:
Molecular Formula:	C15H12FNO
Molecular Weight:	241.2602832

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Identification/Properties

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Chemical Structure

4-(Benzyloxy)-6-fluoro-1H-indole is a versatile compound commonly used in chemical synthesis for various applications. One key application of this compound is its utility as a building block in the synthesis of pharmaceuticals. With its unique structure and functional groups, 4-(Benzyloxy)-6-fluoro-1H-indole serves as a valuable intermediate in the preparation of biologically active molecules. The presence of the benzyl ether and fluoro substituents allows for further derivatization and modification, making it a valuable tool for organic chemists in drug discovery and development. Additionally, the indole moiety in 4-(Benzyloxy)-6-fluoro-1H-indole is a common pharmacophore in many bioactive compounds, further highlighting its significance in chemical synthesis for medicinal chemistry purposes. This compound plays a crucial role in the creation of complex molecules with potential therapeutic applications.