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Atomfair (S)-Allylglycine ethyl ester p-toluenesulfonate C7H13NO2

Description (S)-Allylglycine ethyl ester p-toluenesulfonate (CAS: 1432914-51-6) is a high-purity chiral building block widely used in organic synthesis and pharmaceutical research. This compound, with the molecular formula C7H13NO2, is an ester derivative of (S)-allylglycine, featuring an ethyl ester group and a p-toluenesulfonate counterion for enhanced stability. Its IUPAC name, ethyl (2R)-2-aminopent-4-enoate, reflects its stereochemistry and functional groups, making it valuable for asymmetric synthesis. The compound is supplied as a white to off-white crystalline powder with ??95% purity (HPLC), ensuring consistency for research applications. Proper storage at 2-8??C in a tightly sealed container under inert atmosphere is recommended to maintain stability.…

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Description

Description

(S)-Allylglycine ethyl ester p-toluenesulfonate (CAS: 1432914-51-6) is a high-purity chiral building block widely used in organic synthesis and pharmaceutical research. This compound, with the molecular formula C7H13NO2, is an ester derivative of (S)-allylglycine, featuring an ethyl ester group and a p-toluenesulfonate counterion for enhanced stability. Its IUPAC name, ethyl (2R)-2-aminopent-4-enoate, reflects its stereochemistry and functional groups, making it valuable for asymmetric synthesis. The compound is supplied as a white to off-white crystalline powder with ??95% purity (HPLC), ensuring consistency for research applications. Proper storage at 2-8??C in a tightly sealed container under inert atmosphere is recommended to maintain stability. Suitable for use in peptide synthesis, medicinal chemistry, and as a precursor for bioactive molecules.

  • CAS No: 1432914-51-6
  • Molecular Formula: C7H13NO2
  • Molecular Weight: 143.18
  • Exact Mass: 143.094628657
  • Monoisotopic Mass: 143.094628657
  • IUPAC Name: ethyl (2R)-2-aminopent-4-enoate
  • SMILES: CCOC(=O)[C@@H](CC=C)N
  • Synonyms: (S)-Allylglycine ethyl ester p-toluenesulfonate, ethyl (2R)-2-aminopent-4-enoate, 792907-43-8, (2R)-2-Amino-pent-4-enoicacidethylester, SCHEMBL1770516

Application

(S)-Allylglycine ethyl ester p-toluenesulfonate serves as a key intermediate in the synthesis of non-proteinogenic amino acids and peptidomimetics. Researchers utilize its chiral allyl group for asymmetric C-C bond formation in drug discovery. The compound is also employed in the development of enzyme inhibitors and neurotransmitter analogs due to its structural similarity to natural amino acids.

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