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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)-

1H-Isoindole-1,3(2H)-dione, 2-phenyl-

O=C1N(c2ccccc2)C(=O)c2c1cccc2 Request for Quotation
Chemical Name: 1H-Isoindole-1,3(2H)-dione, 2-phenyl-
CAS Number: 520-03-6
Product Number: AG003HVM(AGN-PC-0JL8BW)
Synonyms:
MDL No:
Molecular Formula: C14H9NO2
Molecular Weight: 223.2268

Identification/Properties

Properties
MP:
204-207 °C
BP:
388.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
223.231g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
223.063g/mol
Monoisotopic Mass:
223.063g/mol
Topological Polar Surface Area:
37.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
309
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


2-Phenylisoindole-1,3-dione, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Its unique structure and reactivity make it a valuable building block for creating various organic molecules. In particular, $name$ is commonly used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its ability to undergo diverse chemical reactions enables chemists to modify its structure and generate novel compounds with desirable properties. Whether employed in the development of new drug candidates or the preparation of advanced materials, 2-Phenylisoindole-1,3-dione plays a crucial role in advancing the field of organic chemistry.