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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-Quinolinamine, 7-(trifluoromethyl)-

Nc1ccnc2c1ccc(c2)C(F)(F)F Request for Quotation
Chemical Name: 4-Quinolinamine, 7-(trifluoromethyl)-
CAS Number: 243666-11-7
Product Number: AG006W29(AGN-PC-0KK7H2)
Synonyms:
MDL No:
Molecular Formula: C10H7F3N2
Molecular Weight: 212.1712

Identification/Properties

Properties
BP:
329.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
212.175g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
212.056g/mol
Monoisotopic Mass:
212.056g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
229
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301-H319
Precautionary Statements:
P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Amino-7-(trifluoromethyl)quinoline is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it a valuable building block for creating a variety of functional molecules. In organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Its trifluoromethyl group enhances the compound's stability and electron density, making it an attractive candidate for reactions requiring strong electron-withdrawing capabilities. Additionally, the amino group provides a site for further functionalization, allowing for the incorporation of diverse chemical functionalities. Furthermore, 4-Amino-7-(trifluoromethyl)quinoline is known for its ability to participate in a range of transformations, such as nucleophilic substitutions, cross-coupling reactions, and heterocyclic synthesis. Its presence in the molecular structure can significantly impact the physicochemical properties of the final products, influencing factors like solubility, bioavailability, and reactivity. This compound's versatility and reactivity make it a valuable tool for chemists seeking to access novel compounds and explore new synthetic pathways.