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Atomfair Phthalimide, N-(2-formylethyl)- C11H9NO3

Description Phthalimide, N-(2-formylethyl)- (CAS No. 2436-29-5) is a high-purity organic compound with the molecular formula C11H9NO3and the IUPAC name 3-(1,3-dioxoisoindol-2-yl)propanal . This specialized chemical features a phthalimide core linked to a propanal group, making it a valuable intermediate in synthetic organic chemistry. With a molecular weight of 203.20 g/mol, it is commonly utilized in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Available in >98% purity (HPLC), this compound is supplied as a crystalline solid with strict quality control to ensure reproducibility in research and industrial applications. Store in a cool, dry place under inert conditions to maintain stability.

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Description

Description

Phthalimide, N-(2-formylethyl)- (CAS No. 2436-29-5) is a high-purity organic compound with the molecular formula C11H9NO3 and the IUPAC name 3-(1,3-dioxoisoindol-2-yl)propanal. This specialized chemical features a phthalimide core linked to a propanal group, making it a valuable intermediate in synthetic organic chemistry. With a molecular weight of 203.20 g/mol, it is commonly utilized in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Available in >98% purity (HPLC), this compound is supplied as a crystalline solid with strict quality control to ensure reproducibility in research and industrial applications. Store in a cool, dry place under inert conditions to maintain stability.

  • CAS No: 2436-29-5
  • Molecular Formula: C11H9NO3
  • Molecular Weight: 203.19
  • Exact Mass: 203.058243149
  • Monoisotopic Mass: 203.058243149
  • IUPAC Name: 3-(1,3-dioxoisoindol-2-yl)propanal
  • SMILES: C1=CC=C2C(=C1)C(=O)N(C2=O)CCC=O
  • Synonyms: 2436-29-5, 3-Phthalimidopropionaldehyde, Phthalimide, N-(2-formylethyl)-, 2H-Isoindole-2-propanal, 1,3-dihydro-1,3-dioxo-, beta-Phthalimidopropionaldehyde

Application

Phthalimide, N-(2-formylethyl)- serves as a versatile building block in organic synthesis, particularly in the preparation of heterocyclic compounds and bioactive molecules. Its reactive aldehyde group enables facile conjugation with amines or hydrazines, making it useful in the development of Schiff bases or hydrazone derivatives. Researchers employ this compound in the synthesis of potential pharmaceutical intermediates, such as enzyme inhibitors or receptor modulators. It is also explored in material science for the design of functionalized polymers and coatings.

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