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Atomfair 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 3,5-dichlorobenzoate C15H7Cl2NO4

Description 1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl 3,5-dichlorobenzoate (CAS No. 2248396-96-3) is a high-purity synthetic organic compound with the molecular formula C15H7Cl2NO4. This specialized chemical features a phthalimide core esterified with a 3,5-dichlorobenzoate group, offering unique reactivity for advanced research applications. With a molecular weight of 336.13 g/mol, this compound is supplied as a crystalline solid with >95% purity (HPLC). Its structural complexity makes it valuable for pharmaceutical intermediates, materials science, and synthetic chemistry studies. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability. For research use only.

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Description

Description

1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl 3,5-dichlorobenzoate (CAS No. 2248396-96-3) is a high-purity synthetic organic compound with the molecular formula C15H7Cl2NO4. This specialized chemical features a phthalimide core esterified with a 3,5-dichlorobenzoate group, offering unique reactivity for advanced research applications. With a molecular weight of 336.13 g/mol, this compound is supplied as a crystalline solid with >95% purity (HPLC). Its structural complexity makes it valuable for pharmaceutical intermediates, materials science, and synthetic chemistry studies. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability. For research use only.

  • CAS No: 2248396-96-3
  • Molecular Formula: C15H7Cl2NO4
  • Molecular Weight: 336.1
  • Exact Mass: 334.9752131
  • Monoisotopic Mass: 334.9752131
  • IUPAC Name: (1,3-dioxoisoindol-2-yl) 3,5-dichlorobenzoate
  • SMILES: C1=CC=C2C(=C1)C(=O)N(C2=O)OC(=O)C3=CC(=CC(=C3)Cl)Cl
  • Synonyms: 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 3,5-dichlorobenzoate, 2248396-96-3, EN300-6514295

Application

This compound serves as a versatile building block in medicinal chemistry for the synthesis of isoindole-1,3-dione derivatives. Researchers utilize it in the development of novel small-molecule inhibitors and bioactive compounds. The dichlorobenzoate moiety provides opportunities for further functionalization in polymer and materials science applications.

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