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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)-

4-(trifluoromethyl)quinolin-2-amine

Nc1nc2ccccc2c(c1)C(F)(F)F Request for Quotation
Chemical Name: 4-(trifluoromethyl)quinolin-2-amine
CAS Number: 211449-19-3
Product Number: AG00C14L(AGN-PC-0NGC2Q)
Synonyms:
MDL No:
Molecular Formula: C10H7F3N2
Molecular Weight: 212.1712

Identification/Properties

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


4-(Trifluoromethyl)quinolin-2-amine is a versatile compound commonly used in chemical synthesis for its unique properties and diverse applications. This compound serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and functional materials.In chemical synthesis, 4-(Trifluoromethyl)quinolin-2-amine is frequently employed as a key intermediate in the preparation of biologically active molecules. Its trifluoromethyl group imparts enhanced lipophilicity and metabolic stability to the final products, making it a desirable moiety in drug design and discovery.Furthermore, the presence of the quinoline ring in 4-(Trifluoromethyl)quinolin-2-amine offers synthetic chemists a powerful scaffold for the modification and functionalization of organic molecules. This structural motif enables the rapid construction of complex molecular architectures with desired pharmacological and physical properties.Overall, the application of 4-(Trifluoromethyl)quinolin-2-amine in chemical synthesis extends beyond its role as a mere reagent; it is a fundamental component in the creation of innovative compounds with broad implications in medicinal chemistry, materials science, and other interdisciplinary fields.