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Catalog Number:
33612
CAS Number:
1217801-44-9
Fmoc-4-(acétyl-amino)-D-phénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
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$62.40 /25 mg
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Product Information

Fmoc-4-(acetyl-amino)-D-phenylalanine 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 amino groups during the synthesis of peptides. Its unique structure, characterized by the acetylamino group and D-phenylalanine, enhances its stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry.

This compound is particularly valuable in the synthesis of bioactive peptides and pharmaceuticals, where precise control over amino acid sequences is crucial. Researchers can leverage Fmoc-4-(acetyl-amino)-D-phenylalanine to create peptides with specific biological activities, paving the way for innovative therapeutic solutions. Its ability to facilitate the formation of complex peptide structures while maintaining high purity levels sets it apart from similar compounds, making it a preferred choice for professionals seeking reliable and effective building blocks in peptide chemistry.

Synonyms
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
CAS Number
1217801-44-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C26H24N2O5
Molecular Weight
444.48
MDL Number
MFCD12198179
PubChem ID
53398091
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = 21,8 ± 2 ° (C = 1 dans DMF)
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
CAS Number
1217801-44-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C26H24N2O5
Molecular Weight
444.48
MDL Number
MFCD12198179
PubChem ID
53398091
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = 21,8 ± 2 ° (C = 1 dans DMF)
Conditions
Conserver entre 2 et 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-4-(acetyl-amino)-D-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides. Its Fmoc protecting group allows for easy removal during the synthesis process, making it ideal for creating complex peptide sequences.
  • Drug Development: In pharmaceutical research, it is used to develop new drugs, particularly in the area of peptide-based therapeutics. Its structure can be modified to enhance bioactivity and selectivity.
  • Bioconjugation: The compound can be employed in bioconjugation techniques, linking peptides to other biomolecules. This is crucial in creating targeted drug delivery systems and improving therapeutic efficacy.
  • Research in Neuroscience: It is utilized in studies related to neuropeptides, which play significant roles in brain function and behavior. This application aids in understanding neurological disorders and developing potential treatments.
  • Custom Synthesis Services: Many research labs and companies offer custom synthesis of this compound, catering to specific research needs. This flexibility is advantageous for researchers requiring tailored compounds for their studies.

Citations