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CS-W001157 4
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2-Amino-N-methyl-N-phenylacetamide

  • CAS No. 126866-37-3

  • Cat. No. CS-0313292
  • Purity≥96%
  • MDL No.None

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

2-Amino-N-methyl-N-phenylacetamide|CS-0313292

Structure of 126866-37-3

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General Information

  • CAS No. 126866-37-3
  • Cat. No. CS-0313292
  • Purity ≥96%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₂N₂O
  • Molecular Weight 164.20
  • Synonym(s) 2-AMINO-N-METHYL-N-PHENYL-ACETAMIDE
  • SMILES CN(C1=CC=CC=C1)C(=O)CN

Description

2-Amino-N-methyl-N-phenylacetamide features a benzene ring conjugated to an amide linkage, delivering enhanced solubility and metabolic stability. The N-methyl group reduces hydrogen bonding potential while the para-amino substituent enables direct functionalization in synthetic routes. This scaffold integrates readily into bioactive molecules requiring balanced lipophilicity and polarity.

Application

2-Amino-N-methyl-N-phenylacetamide serves as a versatile building block in medicinal chemistry, enabling efficient access to diverse amide-linked scaffolds. Its structure features a primary amino group adjacent to a tertiary amide, offering orthogonal reactivity for selective derivatization. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for use in peptide-like conjugations, heterocycle synthesis, and target-oriented compound libraries.

Safety Information

Download SDS
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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   46.33
  • LogP   0.6081
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   2

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