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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)-

5-fluoro-3,4-dihydro-2H-isoquinolin-1-one

O=C1NCCc2c1cccc2F Request for Quotation
Chemical Name: 5-fluoro-3,4-dihydro-2H-isoquinolin-1-one
CAS Number: 230301-83-4
Product Number: AG002LXF(AGN-PC-01V7IS)
Synonyms:
MDL No:
Molecular Formula: C9H8FNO
Molecular Weight: 165.1643

Identification/Properties

Computed Properties
Molecular Weight:
165.167g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
165.059g/mol
Monoisotopic Mass:
165.059g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
195
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Fluoro-3,4-dihydroisoquinolin-1(2H)-one, also known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure and reactivity make it a valuable building block in the creation of various organic molecules through complex chemical reactions.One of the key applications of $name$ in chemical synthesis is as a precursor for the synthesis of biologically active compounds. By utilizing $name$ as a starting material, organic chemists can efficiently introduce the fluorine atom into target molecules, enhancing their biological activity and pharmacological properties.Additionally, $name$ can serve as a key intermediate in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry. Its ability to undergo diverse chemical transformations allows for the efficient construction of complex molecular frameworks, enabling the rapid development of novel drug candidates and agrochemicals.Furthermore, the presence of the fluorine substituent in $name$ can impart unique physicochemical properties to the synthesized compounds, such as altered lipophilicity, enhanced stability, and improved binding affinity to biological targets. This can greatly impact the efficacy and safety profile of the final products, making $name$ an invaluable tool in drug discovery and development.In summary, the strategic use of 5-Fluoro-3,4-dihydroisoquinolin-1(2H)-one in chemical synthesis enables the construction of diverse molecular structures with enhanced biological activity, making it a crucial component in the arsenal of synthetic chemists striving to create innovative compounds with potential therapeutic applications.