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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-fluoro-1H-1,5-naphthyridin-2-one

Fc1cnc2c(c1)[nH]c(=O)cc2 Request for Quotation
Chemical Name: 7-fluoro-1H-1,5-naphthyridin-2-one
CAS Number: 959615-64-6
Product Number: AG00IJOH(AGN-PC-080MIU)
Synonyms:
MDL No:
Molecular Formula: C8H5FN2O
Molecular Weight: 164.1365032

Identification/Properties

Computed Properties
Molecular Weight:
164.139g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
164.039g/mol
Monoisotopic Mass:
164.039g/mol
Topological Polar Surface Area:
42A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
229
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-Fluoro-1,5-naphthyridin-2(1H)-one is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. As an important building block in organic chemistry, this compound serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and functional materials.In chemical synthesis, 7-Fluoro-1,5-naphthyridin-2(1H)-one acts as a valuable starting material for the preparation of heterocyclic compounds with diverse applications. Its fluorine substituent enhances the compound's stability and introduces valuable electronic properties, making it particularly useful in the development of bioactive molecules and organic materials with tailored properties.Additionally, the presence of the naphthyridine ring system in 7-Fluoro-1,5-naphthyridin-2(1H)-one imparts unique structural features that enable further derivatization and functionalization, allowing chemists to explore a wide range of synthetic pathways and opportunities for molecular design.Overall, the application of 7-Fluoro-1,5-naphthyridin-2(1H)-one in chemical synthesis plays a pivotal role in advancing the field of organic chemistry by enabling the efficient and strategic construction of complex molecules with targeted properties and functions.