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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)-

Benzoic acid, 2-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-, methyl ester

COC(=O)c1ccccc1C(=O)ON1C(=O)CCC1=O Request for Quotation
Chemical Name: Benzoic acid, 2-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-, methyl ester
CAS Number: 438470-19-0
Product Number: AG003G0W(AGN-PC-0NCIRE)
Synonyms:
MDL No:
Molecular Formula: C13H11NO6
Molecular Weight: 277.2295

Identification/Properties

Properties
MP:
76 - 80 °C - lit.
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H317
Precautionary Statements:
P280
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,5-Dioxopyrrolidin-1-yl methyl phthalate, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound serves as a key building block in various organic reactions, specifically in the formation of amide linkages. Its unique structure containing a phthalate moiety and a pyrrolidinone ring makes it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. One of the primary applications of 2,5-Dioxopyrrolidin-1-yl methyl phthalate is in peptide synthesis, where it is used as a coupling reagent to facilitate the formation of peptide bonds. Additionally, this compound can also be employed in the preparation of polymers, dyes, and other complex organic molecules due to its ability to act as a versatile reactant in various synthetic pathways. Its compatibility with a wide range of functional groups and the ease of manipulation make it an essential tool for chemists and researchers involved in the development of novel compounds with tailored properties.