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CAS 68123-33-1

:

2,5-Dioxo-1-pyrrolidinyl 4-nitrobenzeneacetate

Description:
2,5-Dioxo-1-pyrrolidinyl 4-nitrobenzeneacetate, identified by its CAS number 68123-33-1, is a chemical compound that features a pyrrolidine ring substituted with both a dioxo group and a nitrobenzeneacetate moiety. This compound typically exhibits characteristics common to both pyrrolidine derivatives and nitro-substituted aromatic compounds. It may display moderate to high solubility in polar organic solvents, while its solid form is likely to be crystalline. The presence of the nitro group suggests potential reactivity, particularly in electrophilic aromatic substitution reactions. Additionally, the dioxo functionality can influence the compound's acidity and reactivity, making it a candidate for various synthetic applications in organic chemistry. The compound's biological activity, if any, would depend on its structural features, potentially allowing for interactions with biological targets. As with many synthetic compounds, safety data should be consulted to understand its handling and toxicity profiles.
Formula:C12H10N2O6
InChI:InChI=1S/C12H10N2O6/c15-10-5-6-11(16)13(10)20-12(17)7-8-1-3-9(4-2-8)14(18)19/h1-4H,5-7H2
InChI key:InChIKey=JUEAHIVORWVODA-UHFFFAOYSA-N
SMILES:O(C(CC1=CC=C(N(=O)=O)C=C1)=O)N2C(=O)CCC2=O
Synonyms:
  • (2,5-Dioxopyrrolidin-1-yl) 2-(4-nitrophenyl)acetate
  • 1-{[(4-Nitrophenyl)Acetyl]Oxy}Pyrrolidine-2,5-Dione
  • 2,5-Dioxo-1-pyrrolidinyl 4-nitrobenzeneacetate
  • 2,5-Pyrrolidinedione, 1-[[(4-nitrophenyl)acetyl]oxy]-
  • Benzeneacetic acid, 4-nitro-, 2,5-dioxo-1-pyrrolidinyl ester
  • N-Succinimidyl 4-nitrophenylacetate
  • NSC 370377
  • Succinimido p-nitrophenylacetate
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