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Catalog Number:
22708
CAS Number:
946727-62-4
Ácido 4-Fmoc-amino-tetrahidrotiopiran-4-il)acético
Purity:
≥ 99 % (HPLC)
Documents
$86.23 /25 mg
Tamaño
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Product Information

(4-Fmoc-amino-tetrahydrothiopyran-4-yl)acetic acid is a versatile compound widely utilized in the field of peptide synthesis and medicinal chemistry. This compound features a unique thian structure that enhances its reactivity and stability, making it an excellent choice for researchers focused on developing novel therapeutic agents. Its Fmoc (9-fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex peptides with high purity and yield.

In practical applications, (4-Fmoc-amino-tetrahydrothiopyran-4-yl)acetic acid is particularly valuable in the design of bioactive peptides and drug candidates, where its structural properties can lead to improved bioavailability and efficacy. Researchers have successfully employed this compound in various studies aimed at understanding protein interactions and developing targeted therapies. Its unique features, such as enhanced solubility and stability, set it apart from similar compounds, making it a preferred choice for professionals in pharmaceutical and biochemical research.

CAS Number
946727-62-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H23NO4S
Molecular Weight
397.49
MDL Number
MFCD09264207
PubChem ID
17040197
Melting Point
144-151 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
946727-62-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H23NO4S
Molecular Weight
397.49
MDL Number
MFCD09264207
PubChem ID
17040197
Melting Point
144-151 ?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-tetrahydrothiopyran-4-yl)acetic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of novel therapeutic agents. Its Fmoc protecting group allows for selective deprotection, facilitating stepwise synthesis.
  • Drug Development: Its unique structure makes it valuable in the design of new drugs, especially in targeting specific biological pathways. Researchers can modify the compound to enhance efficacy and reduce side effects.
  • Bioconjugation: The compound can be used to create bioconjugates, linking drugs to biomolecules for targeted delivery. This application is particularly beneficial in cancer therapy, where precision is crucial.
  • Material Science: It finds applications in developing functional materials, such as hydrogels, which can be used in drug delivery systems. These materials can improve the stability and release profiles of therapeutic agents.
  • Analytical Chemistry: The compound is useful in analytical methods for detecting and quantifying amino acids and peptides, aiding researchers in characterizing complex biological samples.

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