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Catalog Number:
07306
CAS Number:
170642-28-1
Fmoc-D-allyl-Gly-OH
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-2-allylglycine, Acide ( R )-2-(Fmoc-amino)-4-penténoïque, Fmoc-D-Gly(allyl)-OH
Documents
$43.87 /1G
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Product Information

Fmoc-D-allyl-Gly-OH is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique allyl side chain enhances the compound's reactivity and provides opportunities for further functionalization, making it a valuable building block in the design of complex biomolecules. Researchers in medicinal chemistry and biochemistry can leverage Fmoc-D-allyl-Gly-OH to create peptides with specific biological activities, facilitating advancements in therapeutic applications.

The compound's stability under standard laboratory conditions, combined with its ease of use in solid-phase peptide synthesis, makes it an attractive choice for professionals looking to streamline their workflows. Fmoc-D-allyl-Gly-OH is particularly beneficial in the development of peptide-based drugs, where precise control over amino acid sequences is crucial. Its ability to undergo selective reactions allows for the incorporation of diverse functionalities, enhancing the potential for novel therapeutic agents. This compound stands out in the realm of peptide synthesis, offering researchers a reliable and efficient tool for their projects.

Synonyms
Fmoc-D-2-allylglycine, Acide ( R )-2-(Fmoc-amino)-4-penténoïque, Fmoc-D-Gly(allyl)-OH
CAS Number
170642-28-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 20 H 194
Molecular Weight
337.37
MDL Number
MFCD01311776
PubChem ID
4052587
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] 20 D = -9 ± 5 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-D-2-allylglycine, Acide ( R )-2-(Fmoc-amino)-4-penténoïque, Fmoc-D-Gly(allyl)-OH
CAS Number
170642-28-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 20 H 194
Molecular Weight
337.37
MDL Number
MFCD01311776
PubChem ID
4052587
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] 20 D = -9 ± 5 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-D-allyl-Gly-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the design of peptide-based drugs, enhancing their stability and bioavailability, which is essential for pharmaceutical applications.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of peptides to various biomolecules, which is vital in creating targeted therapies.
  • Research in Neuroscience: Researchers utilize it to study neuropeptides, contributing to advancements in understanding neurological functions and disorders.
  • Custom Synthesis: Its versatility allows for custom synthesis of modified peptides, catering to specific research needs in academia and industry.

Citations