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Atomfair Methyl 4-((1S)-1-aminoethyl)benzoate C10H13NO2

Description Methyl 4-((1S)-1-aminoethyl)benzoate (CAS No. 222714-37-6) is a high-purity chiral compound with the molecular formula C10H13NO2. This benzoate derivative features a stereogenic center at the 1-position of the ethylamine side chain, making it a valuable building block for asymmetric synthesis and pharmaceutical research. The compound is supplied as a white to off-white crystalline powder with ??95% purity (HPLC), ensuring consistency for demanding applications. Its well-defined structure, characterized by FTIR, NMR, and mass spectrometry, makes it ideal for use in medicinal chemistry, peptidomimetics, and ligand design. Packaged under inert gas to enhance stability, this product is suited for researchers requiring precise…

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Description

Description

Methyl 4-((1S)-1-aminoethyl)benzoate (CAS No. 222714-37-6) is a high-purity chiral compound with the molecular formula C10H13NO2. This benzoate derivative features a stereogenic center at the 1-position of the ethylamine side chain, making it a valuable building block for asymmetric synthesis and pharmaceutical research. The compound is supplied as a white to off-white crystalline powder with ??95% purity (HPLC), ensuring consistency for demanding applications. Its well-defined structure, characterized by FTIR, NMR, and mass spectrometry, makes it ideal for use in medicinal chemistry, peptidomimetics, and ligand design. Packaged under inert gas to enhance stability, this product is suited for researchers requiring precise chiral intermediates.

  • CAS No: 222714-37-6
  • Molecular Formula: C10H13NO2
  • Molecular Weight: 179.22
  • Exact Mass: 179.094628657
  • Monoisotopic Mass: 179.094628657
  • IUPAC Name: methyl 4-[(1S)-1-aminoethyl]benzoate
  • SMILES: C[C@@H](C1=CC=C(C=C1)C(=O)OC)N
  • Synonyms: 222714-37-6, methyl 4-[(1S)-1-aminoethyl]benzoate, DTXSID40590819, Methyl 4-((1S)-1-aminoethyl)benzoate, DTXCID40541583

Application

Methyl 4-((1S)-1-aminoethyl)benzoate serves as a key chiral synthon in the synthesis of biologically active compounds, particularly for beta-lactam antibiotics and enzyme inhibitors. Its enantiopure structure facilitates the development of stereoselective catalysts and ligands for asymmetric hydrogenation reactions. Researchers also utilize it to introduce chiral benzoyl motifs into peptide backbones for conformational studies.

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