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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)-

Ethanone, 1-(5-bromo-1H-indol-3-yl)-2,2,2-trifluoro-

Brc1ccc2c(c1)c(c[nH]2)C(=O)C(F)(F)F Request for Quotation
Chemical Name: Ethanone, 1-(5-bromo-1H-indol-3-yl)-2,2,2-trifluoro-
CAS Number: 32387-18-1
Product Number: AG00CN2Q(AGN-PC-0KD51U)
Synonyms:
MDL No: MFCD03721051
Molecular Formula: C10H5BrF3NO
Molecular Weight: 292.0520

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H320-H335
Precautionary Statements:
P264-P270-P301+P312-P330
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(5-Bromo-1H-indol-3-yl)-2,2,2-trifluoroethanone, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceuticals. Due to its unique structure and reactivity, $name$ plays a crucial role in the development of novel chemical entities and complex molecular architectures.In chemical synthesis, $name$ is often employed as a key intermediate in the preparation of indole-based compounds. Indoles are ubiquitous in nature and are essential structural motifs in many biologically active molecules, making them valuable targets for synthetic chemists. By utilizing $name$ as a precursor, chemists can access a diverse array of indole derivatives through functional group transformations and cyclization reactions.Additionally, the trifluoroethanone moiety in $name$ presents opportunities for introducing fluorine atoms into organic molecules. Fluorinated compounds exhibit unique physicochemical properties and are highly valuable in medicinal chemistry and material science. By leveraging the trifluoroethanone functionality of $name$, chemists can introduce fluorine atoms selectively at specific positions within a target molecule, thereby modulating its properties and enhancing its biological activity or reactivity.In conclusion, the application of 1-(5-Bromo-1H-indol-3-yl)-2,2,2-trifluoroethanone in chemical synthesis enables the efficient and strategic construction of diverse indole-based compounds and fluorinated molecules with potential applications in drug discovery, agrochemicals, and materials research.