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Catalog Number:
15397
CAS Number:
270263-00-8
Boc-(3-tienil)-Lb-homoalanina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-Lb-HomoAla(3-tienil)-OH, Ácido Boc-( S -3-amino-4-(3-tienil)butírico
Documents
$106.96 /100 mg
Tamaño
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Product Information

Boc-(3-thienyl)-L-b-homoalanine is a versatile amino acid derivative that plays a significant role in peptide synthesis and pharmaceutical research. This compound features a unique thienyl group, which enhances its reactivity and compatibility with various chemical processes. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, making it an ideal choice for researchers looking to synthesize complex peptides with precision. The compound's structure supports its application in drug development, particularly in creating bioactive peptides that can target specific biological pathways.

In addition to its utility in peptide synthesis, Boc-(3-thienyl)-L-b-homoalanine has shown promise in the development of novel therapeutic agents. Its unique properties make it suitable for applications in medicinal chemistry, where it can be utilized to design compounds with improved efficacy and selectivity. Researchers in the fields of biochemistry and pharmacology will find this compound invaluable for exploring new avenues in drug discovery and development, particularly in the creation of targeted therapies.

Synonyms
Boc-Lb-HomoAla(3-tienil)-OH, Ácido Boc-( S -3-amino-4-(3-tienil)butírico
CAS Number
270263-00-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C13H19NO4S
Molecular Weight
285.36
MDL Number
MFCD01861084
PubChem ID
53397989
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
General Information
Synonyms
Boc-Lb-HomoAla(3-tienil)-OH, Ácido Boc-( S -3-amino-4-(3-tienil)butírico
CAS Number
270263-00-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C13H19NO4S
Molecular Weight
285.36
MDL Number
MFCD01861084
PubChem ID
53397989
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Properties
Additional property information coming soon!
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Applications

Boc-(3-thienyl)-L-b-homoalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, particularly in the development of novel therapeutic agents. Its unique structure allows for the incorporation of thienyl groups, enhancing the biological activity of the resulting peptides.
  • Drug Development: It plays a significant role in pharmaceutical research, particularly in the design of drugs targeting specific receptors. The thienyl moiety can improve the binding affinity and selectivity of drug candidates.
  • Bioconjugation: The compound is used in bioconjugation processes, where it can be linked to biomolecules for targeted delivery systems, such as in cancer therapy, enhancing the efficacy of treatments.
  • Research in Neuroscience: Its application extends to neuroscience, where it is investigated for its potential effects on neurotransmitter systems, offering insights into new treatments for neurological disorders.
  • Material Science: The compound is also explored in material science for creating novel polymers and materials with specific electrical or optical properties, leveraging its unique chemical structure.

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