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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)-

1-phenyl-2,4-dihydro-1H-isoquinolin-3-one

O=C1Cc2ccccc2C(N1)c1ccccc1 Request for Quotation
Chemical Name: 1-phenyl-2,4-dihydro-1H-isoquinolin-3-one
CAS Number: 17507-05-0
Product Number: AG002048(AGN-PC-0JKK5P)
Synonyms:
MDL No:
Molecular Formula: C15H13NO
Molecular Weight: 223.2698

Identification/Properties

Computed Properties
Molecular Weight:
223.275g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
223.1g/mol
Monoisotopic Mass:
223.1g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
283
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


1-Phenyl-1,4-dihydroisoquinolin-3(2H)-one, commonly referred to as $name$, serves as a versatile building block in chemical synthesis processes. This compound is recognized for its pivotal role in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it a valuable intermediate for the construction of complex organic molecules. By incorporating $name$ into synthetic routes, chemists can efficiently access a wide range of biologically active compounds with diverse pharmacological properties. Additionally, the selective functionalization of $name$ enables the introduction of specific chemical functionalities, facilitating the design and synthesis of novel molecules with tailored properties. In summary, the application of 1-Phenyl-1,4-dihydroisoquinolin-3(2H)-one in chemical synthesis offers a strategic approach for the efficient and practical synthesis of valuable compounds across various industries.