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CAS 1212257-18-5

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Fmoc-Cyclopropylglycine

Description:
Fmoc-Cyclopropylglycine is a synthetic amino acid derivative characterized by the presence of a cyclopropyl group attached to the glycine backbone, along with a 9-fluorenylmethoxycarbonyl (Fmoc) protective group. This compound is notable for its role in peptide synthesis, particularly in the development of peptides with unique structural and functional properties. The Fmoc group serves as a protecting group for the amino functionality, allowing for selective reactions during peptide assembly. Cyclopropylglycine itself is of interest due to its potential influence on the conformational properties of peptides, which can affect biological activity. The compound is typically used in research and pharmaceutical applications, particularly in the design of peptide-based drugs. Its molecular structure contributes to its unique reactivity and stability, making it a valuable building block in organic synthesis. As with many synthetic compounds, handling precautions should be observed, and its properties should be evaluated in the context of specific applications.
Formula:C20H19NO4
Synonyms:
  • Fmoc-(S)-Amino-cyclopropyl-acetic acid
  • (2S)-2-cyclopropyl-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)acetic acid
  • N-α-(9-Fluorenylmethoxycarbonyl)-L-α-cyclopropylglycine
  • Fmoc-L-cyclopropylglycine≥ 99% (HPLC, Chiral purity)
  • N-Fmoc-S-2-Cyclopropylglycine
  • Fmoc-(S)-2-cyclopropylglycine
  • (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-cyclopropylacetic acid
  • L-2-Cyclopropylglycine, N-FMOC protected, (S)-Cyclopropyl({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)acetic acid
  • (S)-Fmoc-cyclopropylglycine
  • Cyclopropaneacetic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αS)-
  • See more synonyms
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