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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)-

8-fluoroquinolin-3-amine

Nc1cnc2c(c1)cccc2F Request for Quotation
Chemical Name: 8-fluoroquinolin-3-amine
CAS Number: 936324-21-9
Product Number: AG00IHPP(AGN-PC-09GKAG)
Synonyms:
MDL No:
Molecular Formula: C9H7FN2
Molecular Weight: 162.1637

Identification/Properties

Computed Properties
Molecular Weight:
162.167g/mol
XLogP3:
1.5
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:
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


8-Fluoroquinolin-3-amine, also known as $name$, is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. In organic synthesis, $name$ is frequently employed in the formation of diverse molecular structures through the introduction of the fluorine moiety into the desired molecules. Its functional group offers opportunities for selective chemical modifications and derivatization, making it a valuable tool in the construction of complex organic molecules. Additionally, the presence of the quinoline scaffold in $name$ imparts biological activity to its derivatives, making it an important intermediate in the development of new drugs and bioactive compounds. Its role in chemical synthesis extends to the creation of fluorescent probes, molecular imaging agents, and ligands for catalysis. Overall, 8-Fluoroquinolin-3-amine plays a crucial role in advancing the field of chemistry by enabling the synthesis of diverse and functionally important compounds.