🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
15704
CAS Number:
507472-09-5
Acide Fmoc-( S -3-amino-3-(3-thiényl)propionique)
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-β-Ala-(3-thiényl)-OH, ( S -Fmoc-3-thiényl-β-phénylalanine
Documents
$93.14 /100 mg
Taille
Request Bulk Quote
Product Information

Fmoc-(S)-3-amino-3-(3-thienyl)propionic acid is a versatile building block 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 peptides. Its unique thienyl side chain enhances the compound's ability to participate in various chemical reactions, making it particularly valuable in the design of bioactive peptides and pharmaceuticals. Researchers appreciate its stability and compatibility with standard coupling reagents, which facilitates efficient synthesis processes.

In addition to its role in peptide synthesis, Fmoc-(S)-3-amino-3-(3-thienyl)propionic acid has potential applications in the development of novel therapeutics targeting specific biological pathways. Its structural features allow for the exploration of new drug candidates with improved efficacy and selectivity. This compound is ideal for researchers looking to innovate in the fields of medicinal chemistry and biochemistry, providing a reliable option for creating complex molecular architectures.

Synonyms
Fmoc-D-β-Ala-(3-thiényl)-OH, ( S -Fmoc-3-thiényl-β-phénylalanine
CAS Number
507472-09-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 19 NON 4 S
Molecular Weight
393.46
MDL Number
MFCD03427989
PubChem ID
24902260
Melting Point
179-184 ºC
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = -46 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-D-β-Ala-(3-thiényl)-OH, ( S -Fmoc-3-thiényl-β-phénylalanine
CAS Number
507472-09-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 19 NON 4 S
Molecular Weight
393.46
MDL Number
MFCD03427989
PubChem ID
24902260
Melting Point
179-184 ºC
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = -46 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(S)-3-amino-3-(3-thienyl)propionic 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 solid-phase peptide synthesis, allowing for the creation of complex structures with specific functionalities.
  • Drug Development: Its unique thiophene structure enhances the pharmacological properties of peptides, making it valuable in the design of new therapeutic agents targeting various diseases.
  • Bioconjugation: The Fmoc protecting group facilitates selective reactions, enabling researchers to attach biomolecules to peptides, which is crucial in developing targeted drug delivery systems.
  • Research in Neuroscience: Compounds derived from this amino acid are being explored for their potential in modulating neurotransmitter systems, which could lead to advancements in treating neurological disorders.
  • Material Science: Its properties are being investigated for applications in creating novel materials, such as hydrogels, which can be used in tissue engineering and regenerative medicine.

Citations