1. Home
  2. 8-fluoroquinolin-2-amine

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-2-amine

Nc1ccc2c(n1)c(F)ccc2 Request for Quotation
Chemical Name: 8-fluoroquinolin-2-amine
CAS Number: 1342095-20-8
Product Number: AG009YRH(AGN-PC-0FN1YG)
Synonyms:
MDL No:
Molecular Formula: C9H7FN2
Molecular Weight: 162.1637

Identification/Properties

Computed Properties
Molecular Weight:
162.167g/mol
XLogP3:
1.9
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

Request for Quotation

Customer Feedback

Chemical Structure


8-Fluoroquinolin-2-amine, also known as $name$, is a versatile compound widely used in chemical synthesis processes. This compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural properties. Specifically, 8-Fluoroquinolin-2-amine is utilized as a key intermediate in the development of novel therapeutic agents, including antiviral and antimicrobial drugs. Its functional group arrangement makes it a crucial component in the construction of complex molecular frameworks, allowing for the efficient production of diverse chemical derivatives with enhanced biological activities. Additionally, the reactivity of 8-Fluoroquinolin-2-amine enables chemists to perform selective transformations and modifications, facilitating the creation of specialized compounds for targeted applications in the fields of medicinal chemistry and material science. By incorporating 8-Fluoroquinolin-2-amine into synthetic pathways, researchers can access a wide range of structurally diverse molecules with potential biologically relevant properties, making it an indispensable tool in modern chemical synthesis strategies.