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CAS 170642-28-1

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(R)-N-Fmoc-Allylglycine

Description:
(R)-N-Fmoc-Allylglycine is a chemical compound that belongs to the class of amino acids, specifically a derivative of glycine. It features a phenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used in peptide synthesis to protect the amino group during the coupling reactions. The presence of the allyl group introduces a double bond, which can be utilized for further chemical modifications or reactions, making it a versatile building block in organic synthesis and peptide chemistry. This compound is typically used in the synthesis of peptides and other bioactive molecules due to its ability to participate in various coupling reactions while maintaining the integrity of the amino acid structure. Its chirality, indicated by the (R) configuration, is crucial for the biological activity of the resulting peptides. As with many chemical substances, proper handling and storage are essential to maintain its stability and reactivity, and it should be used in accordance with safety guidelines in a laboratory setting.
Formula:C20H18NO4
InChI:InChI=1/C20H19NO4/c1-2-7-18(19(22)23)21-20(24)25-12-17-15-10-5-3-8-13(15)14-9-4-6-11-16(14)17/h2-6,8-11,17-18H,1,7,12H2,(H,21,24)(H,22,23)/p-1/t18-/m1/s1
SMILES:C=CC[C@H](C(=O)[O-])N=C(O)OCC1c2ccccc2c2ccccc12
Synonyms:
  • Fmoc-(R)-2-Allylglycine
  • Fmoc-D-2-Allylglycine
  • Fmoc-D-Allylglycine
  • Fmoc-D-(Allyl)Gly-Oh
  • Fmoc-D-Algly-Oh
  • Fmoc-D-Gly(Allyl)-Oh
  • Fmoc-Alpha-Allyl-D-Gly
  • Fmoc-Allyl-D-Glycine
  • Fmoc-(R)-2-Amino-4-Pentenoic Acid
  • (2R)-2-{[(9H-Fluoren-9-Ylmethoxy)Carbonyl]Amino}Pent-4-Enoate
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