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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)-

7-(trifluoromethyl)-2,3-dihydro-1H-indole

FC(c1cccc2c1NCC2)(F)F Request for Quotation
Chemical Name: 7-(trifluoromethyl)-2,3-dihydro-1H-indole
CAS Number: 959236-00-1
Product Number: AG006A8J(AGN-PC-0NP8JG)
Synonyms:
MDL No:
Molecular Formula: C9H8F3N
Molecular Weight: 187.1617

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-(Trifluoromethyl)indoline is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. It serves as a valuable building block in the development of pharmaceuticals, agrochemicals, and functional materials. In organic synthesis, this molecule can undergo various transformations such as substitution, addition, and cyclization reactions to create complex structures with enhanced biological or physical properties. The trifluoromethyl group at the 7-position imparts valuable hydrophobic and electron-withdrawing characteristics, making 7-(Trifluoromethyl)indoline a valuable tool for the design of novel molecules with improved pharmacokinetic profiles or biological activities. Additionally, this compound is known for its ability to participate in diverse cascade reactions, allowing for the efficient construction of complex molecular frameworks in a single step. Whether as a key intermediate or a strategic functional group, 7-(Trifluoromethyl)indoline plays a crucial role in the synthesis of diverse chemical compounds with potential applications in medicine, agriculture, and materials science.