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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-[2-[[(4-methylphenyl)sulfonyl]oxy]ethyl]-

O=C1N(CCOS(=O)(=O)c2ccc(cc2)C)C(=O)c2c1cccc2 Request for Quotation
Chemical Name: 1H-Isoindole-1,3(2H)-dione, 2-[2-[[(4-methylphenyl)sulfonyl]oxy]ethyl]-
CAS Number: 5460-83-3
Product Number: AG00D7XK(AGN-PC-0JO6W1)
Synonyms:
MDL No:
Molecular Formula: C17H15NO5S
Molecular Weight: 345.3697

Identification/Properties

Properties
BP:
528.5°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

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-(1,3-Dioxoisoindolin-2-yl)ethyl 4-methylbenzenesulfonate is a versatile chemical reagent commonly utilized in organic synthesis for the functionalization of organic molecules. This compound is particularly valued for its ability to act as an electrophilic acylating agent, enabling the introduction of the 2-(1,3-dioxoisoindolin-2-yl)ethyl moiety into various organic substrates.The reactivity of 2-(1,3-Dioxoisoindolin-2-yl)ethyl 4-methylbenzenesulfonate allows for the formation of new carbon-carbon and carbon-heteroatom bonds through acylation reactions. This facilitates the synthesis of a wide range of complex organic compounds with tailored functionalities, making it a valuable tool in the construction of organic molecules with specific properties and applications.Moreover, the presence of the sulfonyl group in the compound enhances its stability and reactivity, providing control over the acylation process and facilitating the purification of the desired products. Overall, the application of 2-(1,3-Dioxoisoindolin-2-yl)ethyl 4-methylbenzenesulfonate in chemical synthesis offers chemists a powerful method for accessing diverse structural motifs and advancing the synthesis of diverse organic compounds.