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Catalog Number:
15858
CAS Number:
1217823-56-7
Boc-(S-α-(2-thiophenylmethyl)-proline
Purity:
≥ 97% (HPLC)
Documents
$127.79 /25MG
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Product Information

Boc-(S)-a-(2-thiophenylmethyl)-proline is a valuable compound in the field of pharmaceutical research and organic synthesis. This amino acid derivative features a protected amine group, making it an ideal building block for the synthesis of peptide-based drugs and biologically active molecules. Its unique thiophenylmethyl side chain enhances its potential for selective interactions in biological systems, which is particularly beneficial in drug design and development. Researchers appreciate its versatility in creating complex structures that can lead to novel therapeutic agents.

In addition to its applications in drug discovery, Boc-(S)-a-(2-thiophenylmethyl)-proline can be utilized in the development of advanced materials and as a chiral auxiliary in asymmetric synthesis. Its ability to facilitate stereoselective reactions makes it an essential tool for chemists aiming to produce enantiomerically pure compounds. The compound's stability and ease of handling further contribute to its appeal in laboratory settings, ensuring that it meets the rigorous demands of modern chemical research.

CAS Number
1217823-56-7
Purity
≥ 97% (HPLC)
Molecular Formula
C15H21NO4S
Molecular Weight
311.4
MDL Number
MFCD06659369
Appearance
White solid
Optical Rotation
[a]D25 = -59 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
CAS Number
1217823-56-7
Purity
≥ 97% (HPLC)
Molecular Formula
C15H21NO4S
Molecular Weight
311.4
MDL Number
MFCD06659369
Appearance
White solid
Optical Rotation
[a]D25 = -59 ± 2º (C=1 in EtOH)
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-(S)-a-(2-thiophenylmethyl)-proline 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 therapeutic agents. Its unique structure enhances the stability and bioactivity of the resulting peptides.
  • Drug Development: Researchers leverage this compound in drug discovery processes, especially for creating novel compounds with potential anti-cancer or anti-inflammatory properties, due to its ability to mimic natural amino acids.
  • Bioconjugation: It is used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, improving the efficacy of drug delivery systems and diagnostic tools.
  • Material Science: The compound finds applications in the development of functional materials, such as polymers and coatings, which can be tailored for specific properties like increased durability or resistance to environmental factors.
  • Research in Neuroscience: Its derivatives are explored in neuroscience research for their potential role in modulating neurotransmitter systems, which could lead to advancements in treatments for neurological disorders.

Citations