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Catalog Number:
22718
CAS Number:
946716-29-6
Fmoc-4-aminomethyl-tetrahydropyran-4-carboxylic acid
Purity:
≥ 99% (HPLC)
Documents
$106.96 /25MG
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Product Information

Fmoc-4-aminomethyl-tetrahydropyran-4-carboxylic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its structure allows for easy incorporation into various synthetic pathways, making it an invaluable tool for researchers in medicinal chemistry and biochemistry. The compound's ability to facilitate the formation of peptide bonds while maintaining stability under various reaction conditions enhances its appeal for both academic and industrial applications.

In addition to its role in peptide synthesis, Fmoc-4-aminomethyl-tetrahydropyran-4-carboxylic acid can be employed in the development of novel pharmaceuticals, particularly those targeting specific biological pathways. Its unique properties enable researchers to explore new therapeutic avenues, making it a critical component in the design of innovative drug candidates. The compound's compatibility with various coupling reagents and its ease of use in solid-phase peptide synthesis further underscore its significance in the field.

CAS Number
946716-29-6
Purity
≥ 99% (HPLC)
Molecular Formula
C22H23NO5
Molecular Weight
381.43
MDL Number
MFCD09264209
PubChem ID
17040207
Melting Point
152-162 °C
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
CAS Number
946716-29-6
Purity
≥ 99% (HPLC)
Molecular Formula
C22H23NO5
Molecular Weight
381.43
MDL Number
MFCD09264209
PubChem ID
17040207
Melting Point
152-162 °C
Appearance
White powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-4-aminomethyl-tetrahydropyran-4-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing chemists to selectively modify amino acids without affecting others. Its stability under various conditions makes it a preferred choice in solid-phase peptide synthesis.
  • Drug Development: In pharmaceutical research, it is used to create complex drug molecules. Its unique structure can enhance the bioavailability and efficacy of therapeutic agents, making it valuable in the development of new medications.
  • Bioconjugation: The compound is effective in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules. This application is crucial in creating targeted drug delivery systems and diagnostic tools.
  • Material Science: In the field of materials science, it is used to modify polymer properties, improving their mechanical strength and thermal stability. This enhances the performance of materials in various industrial applications.
  • Research in Organic Chemistry: It is a key reagent in organic synthesis, facilitating the construction of complex organic molecules. Researchers benefit from its versatility and efficiency in various synthetic pathways.

Citations