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Atomfair 1,3-Dioxoisoindolin-2-yl 2-naphthoate C19H11NO4

Description 1,3-Dioxoisoindolin-2-yl 2-naphthoate (CAS No. 2097675-41-5) is a high-purity organic compound with the molecular formula C19H11NO4. This specialized chemical, also known by its IUPAC name (1,3-dioxoisoindol-2-yl) naphthalene-2-carboxylate , features a unique molecular structure combining a phthalimide moiety with a naphthoate ester group. It is supplied as a fine powder or crystalline solid with ??95% purity (HPLC), ideal for research applications requiring precise organic intermediates. The compound is characterized by its excellent stability under standard laboratory conditions and solubility in common organic solvents such as DMSO, DMF, and dichloromethane. Proper storage recommendations include protection from light and moisture at 2-8??C. This…

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Description

Description

1,3-Dioxoisoindolin-2-yl 2-naphthoate (CAS No. 2097675-41-5) is a high-purity organic compound with the molecular formula C19H11NO4. This specialized chemical, also known by its IUPAC name (1,3-dioxoisoindol-2-yl) naphthalene-2-carboxylate, features a unique molecular structure combining a phthalimide moiety with a naphthoate ester group. It is supplied as a fine powder or crystalline solid with ??95% purity (HPLC), ideal for research applications requiring precise organic intermediates. The compound is characterized by its excellent stability under standard laboratory conditions and solubility in common organic solvents such as DMSO, DMF, and dichloromethane. Proper storage recommendations include protection from light and moisture at 2-8??C. This product is intended for research purposes only and is not for human or veterinary use.

  • CAS No: 2097675-41-5
  • Molecular Formula: C19H11NO4
  • Molecular Weight: 317.3
  • Exact Mass: 317.06880783
  • Monoisotopic Mass: 317.06880783
  • IUPAC Name: (1,3-dioxoisoindol-2-yl) naphthalene-2-carboxylate
  • SMILES: C1=CC=C2C=C(C=CC2=C1)C(=O)ON3C(=O)C4=CC=CC=C4C3=O
  • Synonyms: 2097675-41-5, 1,3-Dioxoisoindolin-2-yl 2-naphthoate, EN300-6516205, 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl naphthalene-2-carboxylate

Application

1,3-Dioxoisoindolin-2-yl 2-naphthoate serves as a versatile building block in organic synthesis, particularly in the development of novel pharmaceutical intermediates. Researchers utilize this compound in the preparation of heterocyclic compounds with potential biological activity. Its unique structure makes it valuable for studying structure-activity relationships in medicinal chemistry programs. The naphthoate ester moiety offers opportunities for further functionalization in polymer chemistry applications.

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