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Catalog Number:
29658
CAS Number:
912354-06-4
Ester de l'acide S -Fmoc-2-amino-5-tert-butoxycarbonyl-hexanedioïque-6- tert -butyle
Purity:
≥ 99,5 % (HPLC chirale)
Documents
$194.99 /25 mg
Taille
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Product Information

(S)-Fmoc-2-amino-5-tert-butoxycarbonyl-hexanedioic acid-6-tert-butyl ester is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is crucial for the selective protection of amines during the synthesis of peptides. Its unique structure, including the tert-butoxycarbonyl (Boc) and tert-butyl ester functionalities, enhances its stability and solubility, making it an excellent choice for researchers in organic chemistry and biochemistry.

This compound is particularly beneficial in the synthesis of complex peptides and can be employed in various applications, including the development of pharmaceuticals and biologically active compounds. Its ability to provide a stable and easily removable protecting group allows for efficient and streamlined synthesis processes. Researchers and industry professionals can leverage (S)-Fmoc-2-amino-5-tert-butoxycarbonyl-hexanedioic acid-6-tert-butyl ester to enhance their peptide synthesis workflows, ultimately leading to more effective drug formulations and therapeutic agents.

CAS Number
912354-06-4
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 30 H 378
Molecular Weight
539.63
MDL Number
MFCD18782832
PubChem ID
73238925
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] 20 D = 6 ± 1 º (C = 0,16 dans CHCl 3 )
Conditions
Conserver à 0 - 8 °C
General Information
CAS Number
912354-06-4
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 30 H 378
Molecular Weight
539.63
MDL Number
MFCD18782832
PubChem ID
73238925
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] 20 D = 6 ± 1 º (C = 0,16 dans CHCl 3 )
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(S)-Fmoc-2-amino-5-tert-butoxycarbonyl-hexanedioic acid-6-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, which are essential in drug development and biotechnology. Its protective groups help in selectively synthesizing complex peptide chains.
  • Drug Development: In pharmaceutical research, it is used to create novel drug candidates, particularly in the development of therapeutics targeting various diseases, including cancer and metabolic disorders.
  • Bioconjugation: The compound is valuable in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents, enhancing their efficacy and targeting capabilities.
  • Research in Protein Engineering: It aids in the modification of proteins, enabling scientists to design proteins with specific functionalities, which is crucial in enzyme engineering and synthetic biology.
  • Analytical Chemistry: This chemical is employed in analytical methods to study the structure and function of biomolecules, providing insights that are critical in both academic and industrial research settings.

Citations