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Catalog Number:
22742
CAS Number:
285996-74-9
Acide Fmoc-1-amino-4-oxo-cyclohexane carboxylique
Purity:
≥ 98 % (HPLC)
Documents
$127.79 /100 mg
Taille
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Product Information

Fmoc-1-amino-4-oxo-cyclohexane carboxylic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethyloxycarbonyl) protective group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its cyclohexane structure contributes to its stability and solubility, making it an excellent choice for researchers focused on developing novel therapeutic agents.

In the pharmaceutical industry, this compound is particularly valuable for its role in the synthesis of cyclic peptides and other complex molecules. Its ability to facilitate the formation of peptide bonds while maintaining structural integrity allows for the creation of diverse and functional peptide libraries. Researchers can leverage Fmoc-1-amino-4-oxo-cyclohexane carboxylic acid to explore new drug candidates, optimize lead compounds, and enhance the efficacy of existing therapies. Its unique properties make it a preferred choice for professionals seeking reliable and efficient solutions in peptide chemistry.

CAS Number
285996-74-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 22 H 215
Molecular Weight
379.41
MDL Number
MFCD02683160
PubChem ID
1268238
Melting Point
144-166 °C
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
General Information
CAS Number
285996-74-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 22 H 215
Molecular Weight
379.41
MDL Number
MFCD02683160
PubChem ID
1268238
Melting Point
144-166 °C
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-1-amino-4-oxo-cyclohexane carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It is used in the design of novel pharmaceuticals, particularly in creating compounds with enhanced bioactivity and stability, making it valuable in medicinal chemistry.
  • Biotechnology: Researchers leverage its properties to develop bioconjugates, which can improve the delivery of therapeutic agents, enhancing efficacy in targeted therapies.
  • Material Science: The compound is applied in the development of advanced materials, such as polymers and nanomaterials, which can be tailored for specific applications in electronics and coatings.
  • Analytical Chemistry: It is utilized in chromatography and mass spectrometry for the analysis of complex mixtures, aiding in the identification and quantification of biomolecules.

Citations