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2-(2-Aminoethyl)isoindoline-1,3-dione hydrochloride

  • CAS No. 30250-67-0

  • Cat. No. CS-0128086
  • Purity≥97%
  • MDL No.MFCD08272836

*For research and further manufacturing use only, not for direct human use.

2-(2-Aminoethyl)isoindoline-1,3-dione hydrochloride|CS-0128086

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General Information

  • CAS No. 30250-67-0
  • Cat. No. CS-0128086
  • Purity ≥97%
  • MDL No. MFCD08272836
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₁ClN₂O₂
  • Molecular Weight 226.66
  • Synonym(s) N-(2-AMino-ethyl)-phthaliMide hydrochloride
  • SMILES O=C1N(CCN)C(C2=C1C=CC=C2)=O.[H]Cl

Description

This bench-stable isoindoline-1,3-dione derivative features a pendant aminoethyl side chain, enabling facile conjugation in bioconjugation workflows. The hydrochloride salt enhances solubility in aqueous media, supporting efficient incorporation into peptide and protein labeling strategies under standard conditions.

Application

2-(2-Aminoethyl)isoindoline-1,3-dione hydrochloride serves as a versatile scaffold for heterocyclic synthesis, enabling efficient access to bioactive molecules through amine-directed functionalization. Its bench-stable hydrochloride salt form enhances handling and solubility, while the pendant primary amine facilitates conjugation reactions and derivatization under mild conditions. Functions effectively in peptide coupling, reductive amination, and transition-metal-catalyzed transformations, making it a practical building block for medicinal chemistry campaigns targeting CNS agents and kinase inhibitors.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   63.4
  • LogP   0.6631
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   2

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