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Catalog Number:
15049
CAS Number:
368866-35-7
Fmoc-4-amino-tetrahydrothiopyran-4-carboxylic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-4-amino-4-carboxytetrahydrothiopyran
Documents
$79.22 /100MG
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Product Information

Fmoc-4-amino-tetrahydrothiopyran-4-carboxylic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative, characterized by its unique thiane ring structure, offers enhanced stability and solubility, making it an ideal choice for researchers focused on developing novel therapeutic agents. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains, facilitating the synthesis of complex peptides with high purity and yield.

In the pharmaceutical industry, Fmoc-4-amino-tetrahydrothiopyran-4-carboxylic acid is particularly valuable for the design of bioactive peptides, which can be used in various applications, including targeted drug delivery and the development of enzyme inhibitors. Its unique properties also enable researchers to explore new avenues in medicinal chemistry, particularly in the creation of compounds with improved bioavailability and reduced side effects. With its robust applications and significant advantages over traditional amino acids, this compound is an essential tool for advancing peptide-based research and development.

Synonyms
Fmoc-4-amino-4-carboxytetrahydrothiopyran
CAS Number
368866-35-7
Purity
≥ 99% (HPLC)
Molecular Formula
C21H21NO4S
Molecular Weight
383.46
MDL Number
MFCD02683143
PubChem ID
1268218
Melting Point
194-201 °C
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-4-amino-4-carboxytetrahydrothiopyran
CAS Number
368866-35-7
Purity
≥ 99% (HPLC)
Molecular Formula
C21H21NO4S
Molecular Weight
383.46
MDL Number
MFCD02683143
PubChem ID
1268218
Melting Point
194-201 °C
Appearance
White powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-4-amino-tetrahydrothiopyran-4-carboxylic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing for the selective modification of amino acids without affecting others, which is crucial for creating complex peptides.
  • Drug Development: It plays a significant role in the development of pharmaceutical compounds, particularly in designing drugs that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The chemical is used in bioconjugation processes, linking biomolecules with therapeutic agents, which is essential for creating targeted therapies in cancer treatment.
  • Research in Neuroscience: It is applied in the synthesis of neuroactive compounds, contributing to studies that explore neurological disorders and potential treatments.
  • Material Science: This compound is also explored in the development of new materials, particularly those that require specific chemical properties for applications in sensors and electronics.

Citations