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Catalog Number:
33654
Acide boc-(2 R ,3 R )-3-amino-2-hydroxy-3- m -tolyl-propionique
Purity:
≥ 98 % (pureté chirale)
Documents
$100.05 /25 mg
Taille
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Product Information

Boc-(2R,3R)-3-amino-2-hydroxy-3-m-tolyl-propionic acid is a versatile amino acid derivative that plays a significant role in pharmaceutical and biochemical research. This compound is recognized for its unique structural features, including the Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility in various solvents. Its chiral centers make it particularly valuable in the synthesis of biologically active molecules, allowing researchers to explore its potential in drug development and peptide synthesis.

The compound's applications extend to the production of peptide-based therapeutics, where it serves as a building block for creating complex structures with specific biological activities. Additionally, its ability to act as a chiral auxiliary makes it a preferred choice for asymmetric synthesis, providing researchers with a reliable tool for developing enantiomerically pure compounds. With its favorable properties and practical applications, Boc-(2R,3R)-3-amino-2-hydroxy-3-m-tolyl-propionic acid is an essential resource for professionals in medicinal chemistry and related fields.

Purity
≥ 98 % (pureté chirale)
Molecular Formula
C 15 H 215
Molecular Weight
295.33
MDL Number
MFCD07363623
Appearance
Solide blanc
Optical Rotation
[a] D 20 = -42,2 ± 2 ° (C = 0,5 dans MeOH)
Conditions
Conserver entre 2 et 8 °C
General Information
Purity
≥ 98 % (pureté chirale)
Molecular Formula
C 15 H 215
Molecular Weight
295.33
MDL Number
MFCD07363623
Appearance
Solide blanc
Optical Rotation
[a] D 20 = -42,2 ± 2 ° (C = 0,5 dans MeOH)
Conditions
Conserver entre 2 et 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-(2R,3R)-3-amino-2-hydroxy-3-m-tolyl-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 selective reactions and enhancing the yield of desired products.
  • Drug Development: It plays a crucial role in the design of pharmaceutical compounds, particularly in the development of new drugs targeting neurological disorders, due to its structural properties.
  • Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted therapies.
  • Research in Enzyme Inhibition: It is valuable in studies aimed at understanding enzyme mechanisms, particularly in the context of inhibiting specific pathways in metabolic diseases.
  • Material Science: The compound finds applications in the development of new materials with specific properties, such as improved biocompatibility for medical devices.

Citations