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Catalog Number:
15048
CAS Number:
285996-72-7
Acide Fmoc-4-amino-tétrahydropyran-4-carboxylique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-4-amino-4-carboxytétrahydropyrane
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$79.22 /100 mg
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Product Information

Fmoc-4-amino-tetrahydropyran-4-carboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which allows for selective deprotection, making it an essential tool for researchers in the field of organic synthesis. Its unique structure, characterized by a tetrahydropyran ring, enhances the stability and solubility of peptides, facilitating their incorporation into various biological assays and drug development processes.

In addition to its role in peptide synthesis, Fmoc-4-amino-tetrahydropyran-4-carboxylic acid has shown potential in the development of novel therapeutic agents, particularly in the areas of anti-cancer and anti-viral research. Its ability to serve as a chiral auxiliary also opens avenues for asymmetric synthesis, providing researchers with a reliable method for producing enantiomerically pure compounds. With its broad applicability and unique properties, this compound is an invaluable asset for professionals seeking to innovate in chemical research and pharmaceutical development.

Synonyms
Fmoc-4-amino-4-carboxytétrahydropyrane
CAS Number
285996-72-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 21 H 215
Molecular Weight
367.4
MDL Number
MFCD02683137
PubChem ID
2756094
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-4-amino-4-carboxytétrahydropyrane
CAS Number
285996-72-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 21 H 215
Molecular Weight
367.4
MDL Number
MFCD02683137
PubChem ID
2756094
Appearance
Poudre blanche
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-4-amino-tetrahydropyran-4-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In medicinal chemistry, it is used to design and synthesize novel drug candidates, particularly in the development of peptide-based therapeutics, enhancing bioavailability and efficacy.
  • Bioconjugation: The compound facilitates the conjugation of peptides to other biomolecules, such as antibodies or enzymes, improving the specificity and effectiveness of targeted therapies in cancer treatment.
  • Material Science: It finds applications in creating functionalized polymers and materials, which can be used in drug delivery systems, providing controlled release and improved therapeutic outcomes.
  • Analytical Chemistry: Researchers utilize this compound in various analytical techniques, including chromatography and mass spectrometry, to analyze complex mixtures and improve the resolution of peptide separations.

Citations