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Catalog Number:
16643
CAS Number:
1217706-09-6
Fmoc-(R-3-Thienylglycine
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-D-(3-thienyl)glycine
Documents
$72.31 /25MG
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Product Information

Fmoc-(R)-3-Thienylglycine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of complex peptides. Its unique thienyl side chain enhances the compound's ability to participate in various chemical reactions, making it an excellent choice for researchers focused on developing novel therapeutic agents.

In addition to its role in peptide synthesis, Fmoc-(R)-3-Thienylglycine has shown promise in the field of medicinal chemistry, particularly in the design of bioactive compounds. Its structural characteristics allow for improved binding interactions in biological systems, which can lead to enhanced efficacy in drug formulations. Researchers in pharmaceutical and biochemical industries will find this compound invaluable for its ability to facilitate the creation of diverse peptide libraries and its potential applications in targeted drug delivery systems.

Synonyms
Fmoc-D-(3-thienyl)glycine
CAS Number
1217706-09-6
Purity
≥ 99% (HPLC)
Molecular Formula
C21H17NO4S
Molecular Weight
379.43
MDL Number
MFCD02682482
PubChem ID
24729667
Melting Point
184-190 °C
Appearance
White powder
Optical Rotation
[a]D25 = -69 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-D-(3-thienyl)glycine
CAS Number
1217706-09-6
Purity
≥ 99% (HPLC)
Molecular Formula
C21H17NO4S
Molecular Weight
379.43
MDL Number
MFCD02682482
PubChem ID
24729667
Melting Point
184-190 °C
Appearance
White powder
Optical Rotation
[a]D25 = -69 ± 2º (C=1 in DMF)
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-(R)-3-Thienylglycine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: Its unique structure contributes to the design of novel pharmaceuticals, particularly in developing compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The chemical is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems.
  • Research in Neuroscience: Fmoc-(R)-3-Thienylglycine is explored for its potential effects on neurotransmitter systems, providing insights into neuropharmacology and the development of treatments for neurological disorders.
  • Material Science: Its properties are being investigated for applications in creating functional materials, such as sensors and catalysts, due to its ability to interact with various substrates.

Citations