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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)-

3-methyl-2-(trifluoromethyl)-1H-indole

Cc1c2ccccc2[nH]c1C(F)(F)F Request for Quotation
Chemical Name: 3-methyl-2-(trifluoromethyl)-1H-indole
CAS Number: 913955-35-8
Product Number: AG00GYLY(AGN-PC-0JTPN2)
Synonyms:
MDL No:
Molecular Formula: C10H8F3N
Molecular Weight: 199.1724

Identification/Properties

Properties
BP:
266.5 °C at 760 mmHg

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Methyl-2-(trifluoromethyl)-1H-indole is a versatile compound widely utilized in chemical synthesis. One key application of this compound is as a valuable building block in the creation of novel pharmaceuticals and agrochemicals. Its unique structure, incorporating both a methyl group and a trifluoromethyl group on the indole ring, makes it a valuable intermediate in the synthesis of biologically active molecules.In organic synthesis, 3-Methyl-2-(trifluoromethyl)-1H-indole can serve as a key starting material for the preparation of various heterocyclic compounds, which are essential in drug discovery and development. The trifluoromethyl group, in particular, imparts unique physicochemical properties to the molecule, enhancing its bioavailability and metabolic stability in potential drug candidates.Furthermore, the presence of a methyl group at the 3-position of the indole ring allows for further functionalization, enabling chemists to introduce additional substituents or linkers to tailor the properties of the final compound. This flexibility in structural modification is crucial in the design of new chemical entities with improved pharmacological profiles.Overall, the use of 3-Methyl-2-(trifluoromethyl)-1H-indole in chemical synthesis highlights its significance as a valuable scaffold for the construction of complex molecules with potential applications in the fields of medicine and agriculture.