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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-7-methoxy-1H-indole

COc1cc(F)cc2c1[nH]cc2 Request for Quotation
Chemical Name: 5-fluoro-7-methoxy-1H-indole
CAS Number: 1227561-74-1
Product Number: AG000JAL(AGN-PC-0JF3U7)
Synonyms:
MDL No:
Molecular Formula: C9H8FNO
Molecular Weight: 165.1643

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H317
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Fluoro-7-methoxy-1H-indole is a versatile chemical compound widely utilized in chemical synthesis processes. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique properties make it a valuable intermediate in the synthesis of diverse organic compounds.In chemical synthesis, 5-Fluoro-7-methoxy-1H-indole can act as a key starting material for the production of novel drug candidates. Its structural features contribute to the development of potent bioactive molecules with potential applications in medicinal chemistry. By incorporating this compound into synthetic routes, chemists can access a wide range of functionalized derivatives with tailored properties and activities.Furthermore, the presence of the fluoro and methoxy substituents in 5-Fluoro-7-methoxy-1H-indole enables selective modifications at specific positions, allowing for precise control over the chemical reactions. This compound's reactivity and compatibility with various reaction conditions make it a valuable tool for generating complex molecular scaffolds with enhanced biological activities.Overall, the strategic utilization of 5-Fluoro-7-methoxy-1H-indole in chemical synthesis highlights its significance in the development of innovative compounds with potential therapeutic, agricultural, and industrial applications.