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Catalog Number:
05726
CAS Number:
159751-47-0
Ester δ- tert -butylique de l'acide Fmoc-L-α-aminoadipique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Aad(OtBu)-OH, Ester δ- tert -butylique de l'acide Fmoc-L-2-aminohexanedioïque
Documents
$127.79 /250 mg
Taille
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Product Information

Fmoc-L-a-aminoadipic acid d-tert-butyl ester is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This compound serves as a protective group for amino acids, facilitating the formation of peptide bonds while ensuring stability during various chemical reactions. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) group, allows for easy removal under mild conditions, making it an ideal choice for researchers aiming to streamline their synthesis processes.

In addition to its role in peptide synthesis, Fmoc-L-a-aminoadipic acid d-tert-butyl ester is also valuable in the development of bioactive compounds and drug candidates. Its ability to enhance solubility and stability of peptides can lead to improved pharmacological properties, making it a preferred choice in medicinal chemistry. Researchers in the fields of biochemistry and pharmaceutical sciences will find this compound particularly beneficial for creating complex peptide structures with high purity and yield.

Synonyms
Fmoc-L-Aad(OtBu)-OH, Ester δ- tert -butylique de l'acide Fmoc-L-2-aminohexanedioïque
CAS Number
159751-47-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 25 H 296
Molecular Weight
439.4
MDL Number
MFCD00237006
PubChem ID
22314653
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-L-Aad(OtBu)-OH, Ester δ- tert -butylique de l'acide Fmoc-L-2-aminohexanedioïque
CAS Number
159751-47-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 25 H 296
Molecular Weight
439.4
MDL Number
MFCD00237006
PubChem ID
22314653
Appearance
Solide blanc à blanc cassé
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-L-a-aminoadipic acid d-tert-butyl 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 (SPPS), allowing for the efficient assembly of complex peptide sequences.
  • Drug Development: Its application in drug design helps create peptide-based therapeutics, which are crucial in treating various diseases, including cancer and metabolic disorders.
  • Bioconjugation: The chemical is used for bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in developing targeted drug delivery systems.
  • Research in Biochemistry: It plays a significant role in biochemical research, particularly in studying protein interactions and functions, aiding researchers in understanding cellular processes.
  • Modification of Amino Acids: This compound allows for the modification of amino acids, enhancing their properties for specific applications in both research and industrial settings, leading to more effective experimental outcomes.

Citations