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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-Amino-6-fluoroquinoline

Fc1ccc2c(c1)c(N)ccn2 Request for Quotation
Chemical Name: 4-Amino-6-fluoroquinoline
CAS Number: 874800-60-9
Product Number: AG004FN1(AGN-PC-0WAKLX)
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


6-Fluoroquinolin-4-amine, also known as $name$, is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. Its application in organic synthesis ranges from pharmaceutical research to material science and agrochemical development. As a primary amine with a fluoro-substituted quinoline backbone, 6-Fluoroquinolin-4-amine serves as a valuable building block for the synthesis of various biologically active molecules and functional materials.One key application of 6-Fluoroquinolin-4-amine is in the development of novel pharmaceutical agents. Its presence in the molecular structure of drug candidates can impart desirable pharmacological properties, such as enhanced bioavailability and target specificity. By incorporating 6-Fluoroquinolin-4-amine into the molecular design of drug analogs, medicinal chemists can explore new avenues for optimizing drug efficacy and reducing potential side effects.Furthermore, 6-Fluoroquinolin-4-amine plays a crucial role in the synthesis of heterocyclic compounds with diverse functionalities. Its ability to participate in various chemical reactions, such as nucleophilic substitution and transition metal-catalyzed coupling reactions, makes it a valuable intermediate for the construction of complex molecular scaffolds. By harnessing the reactivity of 6-Fluoroquinolin-4-amine, chemists can efficiently access structurally diverse compounds with potential applications in medicinal chemistry, materials science, and agrochemical research.In summary, 6-Fluoroquinolin-4-amine is a versatile building block with immense synthetic potential, making it a valuable tool for chemists working in the field of organic chemistry and drug discovery. Its versatility and reactivity open up new possibilities for the design and synthesis of novel molecules with significant implications for various scientific disciplines.