1. Home
  2. Quinoline, 8-fluoro-5-nitro-

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)-

Quinoline, 8-fluoro-5-nitro-

[O-][N+](=O)c1ccc(c2c1cccn2)F Request for Quotation
Chemical Name: Quinoline, 8-fluoro-5-nitro-
CAS Number: 94832-39-0
Product Number: AG00IIL1(AGN-PC-0JPJZ4)
Synonyms:
MDL No:
Molecular Formula: C9H5FN2O2
Molecular Weight: 192.1466

Identification/Properties

Computed Properties
Molecular Weight:
192.149g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
192.034g/mol
Monoisotopic Mass:
192.034g/mol
Topological Polar Surface Area:
58.7A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
231
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#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


8-Fluoro-5-nitroquinoline, a versatile chemical compound, finds extensive application in organic synthesis processes. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique chemical properties. In chemical synthesis, 8-Fluoro-5-nitroquinoline acts as a valuable intermediate, enabling the production of diverse compounds through functional group transformations and intricate molecular rearrangements. Its strategic incorporation into synthetic pathways allows for the efficient and precise formation of complex molecular structures, thereby facilitating the development of novel drug candidates, advanced materials, and bioactive molecules.