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N-Hydroxybenzimidamide hydrochloride

  • CAS No. 99277-23-3

  • Cat. No. CS-0269717
  • Molecule weightNone
  • Purity≥97%
  • MDL No.MFCD06656049

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

N-Hydroxybenzimidamide hydrochloride|CS-0269717

Structure of 99277-23-3

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General Information

  • CAS No. 99277-23-3
  • Cat. No. CS-0269717
  • Purity ≥97%
  • MDL No. MFCD06656049
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₉ClN₂O
  • Molecular Weight None
  • Synonym(s) Benzamidoximehydrochloride
  • SMILES C1=CC=C(C=C1)C(=N)NO.Cl

Description

N-Hydroxybenzimidamide hydrochloride is a bench-stable, moisture-tolerant reagent featuring a reactive N–OH group that facilitates efficient amidation and heterocycle functionalization. This hydroxylamine derivative enables direct coupling in synthetic transformations without requiring pre-activation, streamlining access to bioactive imidazoles and nitrogen-rich scaffolds under standard conditions.

Application

N-Hydroxybenzimidamide hydrochloride serves as a reliable source of the benzimidazolyl nitroxyl (HNO) moiety, enabling direct incorporation into bioactive scaffolds. Its bench-stable crystalline form facilitates handling and purification in synthetic workflows. The compound functions as a versatile building block for heterocyclic systems requiring nitrogen-rich functionalities, with demonstrated compatibility in amide coupling and nucleophilic substitution reactions.

Safety Information

Download SDS
GHS Pictogram : N/A
GHS No : N/A
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : N/A
Precautionary Statements : N/A

Quality Control

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Computational Chemistry Data

  • TPSA   56.11
  • LogP   1.41257
  • H_Acceptors   2
  • H_Donors   3
  • Rotatable_Bonds   1

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