CHEMOS
N-Aminophthalimide

N-Aminophthalimide

Chemical Name

2-aminoisoindole-1,3-dione

N-Aminophthalimide•Nitrogen Compound (Non-heterocyclic)
Structure: N-Aminophthalimide structure, CAS 1875-48-5, MW 162.15
Product No
CH59002
CAS
1875-48-5
MF
C8H6N2O2
MW
162.15
Specification
Catalog No.CH59002
CAS No.1875-48-5
Molecular FormulaC8H6N2O2
Molecular Weight162.15

CHEMOS Support for This Category

CHEMOS supports non-heterocyclic nitrogen building blocks, including amines, amino alcohols, nitriles, carbamates, and protected intermediates. Chiral amine chemistry : chiral-pool synthesis, resolution, and stereochemical-control strategies. Protecting-group chemistry : Boc, Cbz, Fmoc, and tailored protection or deprotection sequences. Reactive intermediate handling : project-specific safety review for amines, nitriles, and related functional groups. Analytical support : identity, purity, water content, and residual-solvent testing can be discussed. Process development : route refinement and scale-up planning according to target specification.

Overview

N-Aminophthalimide (also known as 2-aminoisoindole-1,3-dione) (CAS 1875-48-5, MF C8H6N2O2, MW 162.15) is a nitrogen-functionalised organic intermediate used in medicinal chemistry and ligand synthesis. Programs working with this compound usually examine route flexibility for downstream substitution, stereo-purity, and impurity control. Project scale-up and custom synthesis are coordinated by the CHEMOS R&D team across laboratory and production sites.

Applications

  • N-Aminophthalimide (1875-48-5) as a starting point for downstream chemistry programs
  • Chiral amine / amino-alcohol research for asymmetric synthesis
  • Custom synthesis of N-protected variants on request
  • Process-development support for scalable preparation

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