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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-Isoindol-1-one, 2,3-dihydro-4-hydroxy-

O=C1NCc2c1cccc2O Request for Quotation
Chemical Name: 1H-Isoindol-1-one, 2,3-dihydro-4-hydroxy-
CAS Number: 366453-21-6
Product Number: AG00C6OC(AGN-PC-00AHJC)
Synonyms:
MDL No:
Molecular Formula: C8H7NO2
Molecular Weight: 149.1467

Identification/Properties

Computed Properties
Molecular Weight:
149.149g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
149.048g/mol
Monoisotopic Mass:
149.048g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
181
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


4-Hydroxy-2,3-dihydroisoindol-1-one, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structural properties make it a valuable tool in the development of novel compounds with potential therapeutic applications. In chemical synthesis, $name$ can be used as a starting material for the synthesis of heterocyclic compounds, which are widely used in drug discovery and development. Its reactivity allows for the introduction of a variety of functional groups, enabling the creation of diverse molecular structures. Additionally, $name$ can undergo various transformations, such as oxidation, reduction, and substitution reactions, making it a valuable precursor in the synthesis of complex molecules. Its utility in chemical synthesis extends to the preparation of advanced materials and the study of new chemical reactions, making it an indispensable component in modern organic chemistry research.