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Catalog Number:
22710
CAS Number:
946716-25-2
Ácido 4-Fmoc-amino-tetrahidropiran-4-il)acético
Purity:
≥ 97 % (HPLC)
Documents
$127.79 /100 mg
Tamaño
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Product Information

(4-Fmoc-amino-tetrahydropyran-4-yl)acetic acid is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique structure that combines the stability of tetrahydropyran with the protective Fmoc (fluorenylmethyloxycarbonyl) group, making it an excellent choice for researchers looking to enhance the efficiency of their synthetic pathways. Its ability to serve as a building block in the development of bioactive peptides allows for the exploration of various therapeutic applications, particularly in drug discovery and development.

In addition to its role in peptide synthesis, (4-Fmoc-amino-tetrahydropyran-4-yl)acetic acid can be employed in the design of novel drug candidates, particularly those targeting specific biological pathways. The compound's favorable properties, including its solubility and stability, make it an attractive option for researchers aiming to optimize their formulations. With its potential to streamline synthesis and improve the efficacy of therapeutic agents, this compound stands out as a valuable asset in both academic and industrial settings.

CAS Number
946716-25-2
Purity
≥ 97 % (HPLC)
Molecular Formula
C22H23NO5
Molecular Weight
381.43
MDL Number
MFCD09264206
PubChem ID
17040199
Melting Point
160-171 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
946716-25-2
Purity
≥ 97 % (HPLC)
Molecular Formula
C22H23NO5
Molecular Weight
381.43
MDL Number
MFCD09264206
PubChem ID
17040199
Melting Point
160-171 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(4-Fmoc-amino-tetrahydropyran-4-yl)acetic 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.
  • Drug Development: It plays a crucial role in the design of new pharmaceuticals, particularly in creating compounds that can enhance bioavailability and stability in drug formulations.
  • Bioconjugation: The chemical is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in developing targeted therapies.
  • Research in Organic Chemistry: Researchers utilize this compound for studying reaction mechanisms and developing new synthetic pathways, contributing to advancements in organic synthesis techniques.
  • Material Science: It is applied in creating functionalized polymers and materials, enhancing properties such as solubility and mechanical strength, which are valuable in various industrial applications.

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