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Catalog Number:
12434
CAS Number:
204246-17-3
Ester α-allylique de l'acide Fmoc-D-aspartique
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-D-Asp-OTout
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Product Information

Fmoc-D-aspartic acid a-allyl ester is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This derivative of aspartic acid features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which allows for selective deprotection during the synthesis of peptides, making it an essential building block for researchers in the field of biochemistry. Its a-allyl ester functionality enhances its reactivity, facilitating the formation of complex peptide structures. This compound is particularly valuable in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial for achieving desired biological activity.

In addition to its applications in peptide synthesis, Fmoc-D-aspartic acid a-allyl ester has shown potential in various research areas, including drug discovery and development. Its unique properties allow for the exploration of new therapeutic avenues, particularly in neuropharmacology, where aspartic acid derivatives play a significant role in neurotransmission. Researchers can leverage this compound to create novel peptides that target specific receptors, potentially leading to breakthroughs in treating neurological disorders. With its robust profile and practical applications, Fmoc-D-aspartic acid a-allyl ester stands out as a key reagent for professionals seeking to innovate in peptide chemistry.

Synonyms
Fmoc-D-Asp-OTout
CAS Number
204246-17-3
Purity
≥ 97 % (HPLC)
Molecular Formula
C 22 H 216
Molecular Weight
395.4
MDL Number
MFCD01074689
PubChem ID
2802354
Appearance
Poudre cristalline blanche ou poudre blanche
Optical Rotation
[a] D 20 = 24 ± 2 º (C = 1 dans DMF)
Conditions
Conserver à ≤ -4 °C
General Information
Synonyms
Fmoc-D-Asp-OTout
CAS Number
204246-17-3
Purity
≥ 97 % (HPLC)
Molecular Formula
C 22 H 216
Molecular Weight
395.4
MDL Number
MFCD01074689
PubChem ID
2802354
Appearance
Poudre cristalline blanche ou poudre blanche
Optical Rotation
[a] D 20 = 24 ± 2 º (C = 1 dans DMF)
Conditions
Conserver à ≤ -4 °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-aspartic acid a-allyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex and biologically active peptides.
  • Drug Development: It plays a significant role in medicinal chemistry, where it is used to develop new pharmaceuticals, especially those targeting neurological disorders due to its structural similarity to neurotransmitters.
  • Bioconjugation: The compound is employed in bioconjugation techniques, enabling researchers to attach biomolecules to surfaces or other molecules, enhancing the functionality of drugs and diagnostics.
  • Research in Neuroscience: It is utilized in studies related to synaptic transmission and neuropharmacology, helping scientists understand the mechanisms of action of various neurotransmitters.
  • Custom Synthesis: The versatility of this compound allows for its use in custom synthesis projects, catering to specific research needs in both academic and industrial settings.

Citations