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Catalog Number:
15016
CAS Number:
342888-28-2
Boc-(S-3-amino-2-(phenylsulfonylamino)propionic acid
Purity:
≥ 99% (HPLC)
Documents
$106.96 /250MG
Pack Size Availability Price
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Product Information

Boc-(S)-3-amino-2-(phenylsulfonylamino)propionic acid is a versatile compound widely utilized in pharmaceutical research and development. This amino acid derivative features a protective Boc (tert-butyloxycarbonyl) group, making it an ideal building block for peptide synthesis and medicinal chemistry applications. Its unique structure, which includes a phenylsulfonylamino group, enhances its reactivity and selectivity in various chemical reactions, facilitating the development of novel therapeutic agents. Researchers often employ this compound in the synthesis of bioactive peptides and small molecules, contributing to advancements in drug discovery and development.

The compound's stability and compatibility with various reaction conditions make it particularly valuable in the synthesis of complex molecules. Its applications extend to the development of inhibitors and modulators in biological systems, showcasing its potential in treating diseases such as cancer and autoimmune disorders. With its robust profile, Boc-(S)-3-amino-2-(phenylsulfonylamino)propionic acid stands out as a crucial tool for researchers aiming to innovate in the field of medicinal chemistry.

CAS Number
342888-28-2
Purity
≥ 99% (HPLC)
Molecular Formula
C14H20N2O6S
Molecular Weight
344.38
MDL Number
MFCD04112668
PubChem ID
4712511
Melting Point
135-140 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -58 ± 2º (C=1 in 1M NaOH)
Conditions
Store at 0-8 °C
General Information
CAS Number
342888-28-2
Purity
≥ 99% (HPLC)
Molecular Formula
C14H20N2O6S
Molecular Weight
344.38
MDL Number
MFCD04112668
PubChem ID
4712511
Melting Point
135-140 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -58 ± 2º (C=1 in 1M NaOH)
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)-3-amino-2-(phenylsulfonylamino)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for drug development and biological studies.
  • Drug Discovery: Its unique properties make it valuable in the pharmaceutical industry for the design of new drugs, particularly those targeting specific biological pathways.
  • Bioconjugation: The chemical is used in bioconjugation processes, linking biomolecules to enhance their therapeutic efficacy or to create targeted delivery systems.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, providing insights into neurological disorders and potential treatments.
  • Analytical Chemistry: This compound is employed in analytical methods to detect and quantify amino acids and related compounds, aiding in quality control and research applications.

Citations