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Catalog Number:
15395
CAS Number:
270262-98-1
Fmoc-(2-thiényl)-L-β-homoalanine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-β-HomoAla(2-thiényl)-OH, Acide Fmoc-( S -3-amino-4-(2-thiényl)butyrique)
Documents
$86.23 /25 mg
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Product Information

Fmoc-(2-thienyl)-L-b-homoalanine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a unique thienyl group, which enhances its reactivity and versatility in various chemical reactions. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains while providing stability during synthesis. Researchers and industry professionals utilize Fmoc-(2-thienyl)-L-b-homoalanine in the development of novel peptides, particularly in the fields of medicinal chemistry and biochemistry, where it can be employed to create compounds with improved biological activity or specificity.

The compound's distinctive properties make it an excellent choice for applications in the pharmaceutical industry, especially in the design of targeted therapies and drug candidates. Its ability to facilitate the synthesis of complex peptide structures opens up possibilities for innovative treatments and research advancements. With its favorable characteristics, Fmoc-(2-thienyl)-L-b-homoalanine stands out as a valuable tool for scientists aiming to explore new frontiers in peptide-based research.

Synonyms
Fmoc-L-β-HomoAla(2-thiényl)-OH, Acide Fmoc-( S -3-amino-4-(2-thiényl)butyrique)
CAS Number
270262-98-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C 23 H 21 NON 4 S
Molecular Weight
407.48
MDL Number
MFCD01861082
PubChem ID
53397986
Melting Point
120 - 124 ?C
Appearance
Poudre brunâtre
Optical Rotation
[a] D 25 = + 10 ± 2 ° (C = 1 dans DMF)
Conditions
Conserver à 0-8°C
General Information
Synonyms
Fmoc-L-β-HomoAla(2-thiényl)-OH, Acide Fmoc-( S -3-amino-4-(2-thiényl)butyrique)
CAS Number
270262-98-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C 23 H 21 NON 4 S
Molecular Weight
407.48
MDL Number
MFCD01861082
PubChem ID
53397986
Melting Point
120 - 124 ?C
Appearance
Poudre brunâtre
Optical Rotation
[a] D 25 = + 10 ± 2 ° (C = 1 dans DMF)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(2-thienyl)-L-b-homoalanine 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 researchers to create complex peptide structures efficiently.
  • Drug Development: Its unique thiophene structure can enhance the biological activity of peptides, making it valuable in the pharmaceutical industry for developing new therapeutics.
  • Bioconjugation: The Fmoc protecting group allows for selective reactions, facilitating the attachment of biomolecules in bioconjugation applications, which is crucial for creating targeted drug delivery systems.
  • Research in Protein Engineering: This compound is used in studies aimed at modifying protein interactions, which can lead to advancements in enzyme design and protein functionality.
  • Material Science: Its properties make it suitable for developing novel materials, including conducting polymers and sensors, which can be applied in electronics and environmental monitoring.

Citations