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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-Fluoroquinolin-4-amine

Fc1ccc2c(c1)nccc2N Request for Quotation
Chemical Name: 7-Fluoroquinolin-4-amine
CAS Number: 948293-49-0
Product Number: AG00IIKN(AGN-PC-0WCZ69)
Synonyms:
MDL No:
Molecular Formula: C9H7FN2
Molecular Weight: 162.1637

Identification/Properties

Computed Properties
Molecular Weight:
162.167g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
162.059g/mol
Monoisotopic Mass:
162.059g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
163
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Fluoroquinolin-4-amine is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials due to its structural characteristics and functional groups.One of the main applications of 7-Fluoroquinolin-4-amine in chemical synthesis is its role as a precursor in the synthesis of biologically active compounds. By modifying and functionalizing the amine group and the fluorine atom in the molecule, chemists can create a diverse array of complex molecules with enhanced medicinal properties. This compound is particularly valuable in the development of new drugs and therapeutic agents, as its structure can be manipulated to improve biological activity and optimize pharmacokinetic properties.Additionally, 7-Fluoroquinolin-4-amine is utilized in the synthesis of fluorescent dyes and markers. By incorporating this compound into fluorescent molecules, scientists can create probes and labels for various biological and analytical applications. The fluorine atom imparts unique spectral properties to the synthesized dyes, making them highly valuable for bioimaging, biosensing, and tracing specific molecules in complex systems.Furthermore, the presence of the quinoline ring in 7-Fluoroquinolin-4-amine offers opportunities for creating functional materials with specific electronic and optical properties. By leveraging the quinoline scaffold, chemists can design and synthesize polymers, liquid crystals, and other advanced materials with tailored characteristics for applications in optoelectronics, sensors, and molecular electronics.Overall, 7-Fluoroquinolin-4-amine plays a crucial role in chemical synthesis by enabling the construction of diverse compounds, from pharmaceuticals to functional materials, with a wide range of applications in various scientific fields.