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Catalog Number:
15017
CAS Number:
16947-86-7
Acide boc-( S -3-amino-2-(p-toluènesulfonylamino)propionique
Purity:
≥ 99 % (HPLC)
Documents
$86.23 /100 mg
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Product Information

Boc-(S)-3-amino-2-(p-toluenesulfonylamino)propionic acid is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This amino acid derivative features a protective Boc (tert-butyloxycarbonyl) group, enhancing its stability and facilitating its use in peptide synthesis. Its unique structure allows for the selective introduction of the p-toluenesulfonyl group, which is crucial for the development of various biologically active compounds. Researchers and industry professionals leverage this compound for its ability to serve as a building block in the synthesis of peptides and other complex molecules, particularly in drug development and biochemical research.

The compound's properties make it particularly advantageous for applications in pharmaceutical research, where it can be employed to create targeted therapies and improve drug efficacy. Its compatibility with various coupling reactions and ability to protect amino groups during synthesis processes further highlight its utility. With its robust performance in peptide synthesis and potential for creating novel therapeutic agents, Boc-(S)-3-amino-2-(p-toluenesulfonylamino)propionic acid stands out as a valuable tool for researchers aiming to innovate in drug discovery and development.

CAS Number
16947-86-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C15H22N2O6S
Molecular Weight
358.41
MDL Number
MFCD04112669
PubChem ID
4712512
Melting Point
120-126 ?C
Appearance
Poudre cristalline blanche
Optical Rotation
[α] D 20
Conditions
Conserver à 0-8 °C
General Information
CAS Number
16947-86-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C15H22N2O6S
Molecular Weight
358.41
MDL Number
MFCD04112669
PubChem ID
4712512
Melting Point
120-126 ?C
Appearance
Poudre cristalline blanche
Optical Rotation
[α] D 20
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-(S)-3-amino-2-(p-toluenesulfonylamino)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids. Its stability under various reaction conditions makes it a preferred choice for chemists.
  • Drug Development: It plays a crucial role in the design of bioactive compounds, particularly in pharmaceuticals targeting specific biological pathways. Researchers leverage its properties to enhance drug efficacy and selectivity.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the performance of diagnostic tools and therapeutic agents.
  • Research in Neuroscience: It is applied in the synthesis of compounds that can modulate neurotransmitter systems, aiding in the development of treatments for neurological disorders.
  • Analytical Chemistry: This chemical is utilized in the development of analytical methods for detecting and quantifying amino acids and peptides, providing valuable insights in various research fields.

Citations