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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)-

4H-Isoindol-4-one, octahydro-2-(phenylmethyl)-

O=C1CCCC2C1CN(C2)Cc1ccccc1 Request for Quotation
Chemical Name: 4H-Isoindol-4-one, octahydro-2-(phenylmethyl)-
CAS Number: 879687-90-8
Product Number: AG00H2QL(AGN-PC-0559SB)
Synonyms:
MDL No:
Molecular Formula: C15H19NO
Molecular Weight: 229.3175

Identification/Properties

Computed Properties
Molecular Weight:
229.323g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
229.147g/mol
Monoisotopic Mass:
229.147g/mol
Topological Polar Surface Area:
20.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
283
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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


2-Benzylhexahydro-1H-isoindol-4(2H)-one, commonly known as $name$, is a versatile compound frequently utilized in chemical synthesis processes. This highly functional molecule serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials due to its unique structural properties.One of the prominent applications of 2-Benzylhexahydro-1H-isoindol-4(2H)-one in chemical synthesis is its role as a precursor in the preparation of biologically active molecules. By incorporating this compound into synthetic routes, chemists can access a diverse range of pharmacologically relevant structures with potential therapeutic benefits. Additionally, the reactivity of 2-Benzylhexahydro-1H-isoindol-4(2H)-one allows for the introduction of substituents and functional groups, enabling fine-tuning of the desired properties of the final product.Moreover, 2-Benzylhexahydro-1H-isoindol-4(2H)-one serves as a valuable intermediate in the synthesis of complex natural products and target compounds. Its strategic placement within multi-step synthetic sequences facilitates the construction of molecular frameworks with high structural complexity and stereochemical precision. This compound's compatibility with various catalytic processes and functional group manipulations further enhances its utility in advancing synthetic methodologies and enabling efficient compound synthesis.