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Catalog Number:
11608
CAS Number:
78512-39-7 
Boc-β-(2-thienyl)-DL-alanine
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-3-DL-Ala(2-thienyl)-OH
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Product Information

Boc-b-(2-thienyl)-DL-alanine is a versatile amino acid derivative that plays a significant role in peptide synthesis and medicinal chemistry. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and facilitates its use in various chemical reactions. Its unique thiophene ring structure contributes to its potential in developing novel pharmaceuticals, particularly in the fields of anti-cancer and anti-inflammatory agents. Researchers appreciate its ability to serve as a building block in the synthesis of complex peptides, enabling the exploration of new therapeutic avenues.

In addition to its applications in drug development, Boc-b-(2-thienyl)-DL-alanine is also utilized in the creation of functional materials and bioactive compounds. Its favorable solubility and reactivity make it an attractive choice for chemists looking to innovate in areas such as organic synthesis and materials science. By incorporating this compound into their research, professionals can unlock new possibilities in the design of targeted therapies and advanced materials, making it a valuable addition to any laboratory.

Synonyms
Boc-3-DL-Ala(2-thienyl)-OH
CAS Number
78512-39-7 
Purity
≥ 98% (HPLC)
Molecular Formula
C12H17NO4S
Molecular Weight
271.3
MDL Number
MFCD00237537
PubChem ID
5035100
Melting Point
111-117 °C
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-3-DL-Ala(2-thienyl)-OH
CAS Number
78512-39-7 
Purity
≥ 98% (HPLC)
Molecular Formula
C12H17NO4S
Molecular Weight
271.3
MDL Number
MFCD00237537
PubChem ID
5035100
Melting Point
111-117 °C
Appearance
White powder
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

Boc-b-(2-thienyl)-DL-alanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require thienyl side chains, enhancing the structural diversity of peptide libraries.
  • Drug Development: It is employed in the development of novel pharmaceuticals, especially in designing compounds that target specific biological pathways, leveraging the unique properties of the thienyl group.
  • Bioconjugation: The compound can be used in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in drug delivery systems.
  • Research in Neuroscience: Its derivatives are investigated for their potential neuroprotective effects, making it relevant in studies aimed at developing treatments for neurodegenerative diseases.
  • Analytical Chemistry: Boc-b-(2-thienyl)-DL-alanine is utilized in analytical methods for detecting and quantifying amino acids in biological samples, providing essential data for biochemical research.

Citations