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Atomfair 2-(Dibenzylamino)acetic acid C16H17NO2

Description 2-(Dibenzylamino)acetic acid (CAS No. 17360-47-3) is a high-purity organic compound with the molecular formula C16H17NO2. This white to off-white crystalline powder is a derivative of glycine, featuring dibenzylamino substitution, which enhances its utility in synthetic organic chemistry and pharmaceutical research. With a molecular weight of 255.31 g/mol, it exhibits excellent solubility in polar organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO), making it ideal for laboratory-scale reactions. This compound is rigorously tested via HPLC, NMR, and mass spectrometry to ensure ??98% purity, meeting the stringent requirements of researchers and industrial applications. Proper storage at 2-8??C in a…

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Description

Description

2-(Dibenzylamino)acetic acid (CAS No. 17360-47-3) is a high-purity organic compound with the molecular formula C16H17NO2. This white to off-white crystalline powder is a derivative of glycine, featuring dibenzylamino substitution, which enhances its utility in synthetic organic chemistry and pharmaceutical research. With a molecular weight of 255.31 g/mol, it exhibits excellent solubility in polar organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO), making it ideal for laboratory-scale reactions. This compound is rigorously tested via HPLC, NMR, and mass spectrometry to ensure ??98% purity, meeting the stringent requirements of researchers and industrial applications. Proper storage at 2-8??C in a tightly sealed container ensures long-term stability.

  • CAS No: 17360-47-3
  • Molecular Formula: C16H17NO2
  • Molecular Weight: 255.31
  • Exact Mass: 255.125928785
  • Monoisotopic Mass: 255.125928785
  • IUPAC Name: 2-(dibenzylamino)acetic acid
  • SMILES: C1=CC=C(C=C1)CN(CC2=CC=CC=C2)CC(=O)O
  • Synonyms: 2-(dibenzylamino)acetic acid, 958-536-4, 17360-47-3, (Dibenzylamino)acetic acid, Glycine, N,N-bis(phenylmethyl)-

Application

2-(Dibenzylamino)acetic acid serves as a versatile building block in the synthesis of peptidomimetics and bioactive molecules, particularly in medicinal chemistry for drug discovery. It is employed as an intermediate in the preparation of chiral ligands for asymmetric catalysis, enhancing enantioselective reactions. Researchers also utilize it to modify peptide backbones, improving metabolic stability and binding affinity in therapeutic candidates.

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