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Catalog Number:
15324
CAS Number:
269726-89-8
Boc-(2-thiényl)-D-β-homoalanine
Purity:
≥ 98%
Synonym(s):
Boc-D-β-HomoAla(2-thiényl)-OH, Acide boc-( R -3-amino-4-(2-thiényl)butyrique
Documents
$100.05 /100 mg
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Product Information

Boc-(2-thienyl)-D-b-homoalanine is a specialized amino acid derivative that plays a significant role in peptide synthesis and pharmaceutical development. This compound features a unique thienyl group, which enhances its bioactivity and offers potential applications in drug design, particularly in the development of novel therapeutics targeting various diseases. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, making it an ideal candidate for use in solid-phase peptide synthesis, where precision and efficiency are paramount.

Researchers and industry professionals can leverage Boc-(2-thienyl)-D-b-homoalanine in the creation of peptides with enhanced stability and specificity. Its unique structure can facilitate the design of compounds with improved pharmacokinetic properties, making it valuable in medicinal chemistry. Additionally, this compound can be utilized in the synthesis of biologically active molecules, contributing to advancements in drug discovery and development. With its distinctive features and practical applications, Boc-(2-thienyl)-D-b-homoalanine stands out as a versatile tool for researchers aiming to innovate in the field of peptide chemistry.

Synonyms
Boc-D-β-HomoAla(2-thiényl)-OH, Acide boc-( R -3-amino-4-(2-thiényl)butyrique
CAS Number
269726-89-8
Purity
≥ 98%
Molecular Formula
C 13 H 19 NON 4 S
Molecular Weight
285.36
MDL Number
MFCD01860984
PubChem ID
53397911
Melting Point
90-96 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = -7 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-D-β-HomoAla(2-thiényl)-OH, Acide boc-( R -3-amino-4-(2-thiényl)butyrique
CAS Number
269726-89-8
Purity
≥ 98%
Molecular Formula
C 13 H 19 NON 4 S
Molecular Weight
285.36
MDL Number
MFCD01860984
PubChem ID
53397911
Melting Point
90-96 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = -7 ± 2º (C=1 dans EtOH)
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

Boc-(2-thienyl)-D-b-homoalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of therapeutics targeting specific biological pathways.
  • Drug Development: Its unique structural properties make it an important candidate in the design of novel drugs, especially in the field of oncology and neuropharmacology.
  • Bioconjugation: The compound can be used in bioconjugation processes, allowing researchers to attach biomolecules to drugs, enhancing their efficacy and targeting capabilities.
  • Research on Protein Interactions: It aids in studying protein-ligand interactions, providing insights into molecular mechanisms that can lead to new therapeutic strategies.
  • Material Science: The compound is also explored in the development of advanced materials, such as sensors and catalysts, due to its unique electronic properties.

Citations