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Catalog Number:
33672
CAS Number:
1217672-32-6, 1391393-11-5
Acide boc-(2 R ,3 R )-3-amino-2-hydroxy-3-(3-méthoxyphényl)propionique
Purity:
≥ 98 % (pureté chirale)
Documents
$120.00 /25 mg
Taille
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Product Information

Boc-(2R,3R)-3-amino-2-hydroxy-3-(3-methoxyphenyl)propionic acid is a versatile compound widely utilized in pharmaceutical research and development. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal candidate for peptide synthesis and drug formulation. Its unique structure, characterized by the presence of a methoxyphenyl group, allows for specific interactions in biological systems, facilitating the design of targeted therapies. Researchers have found it particularly useful in the development of novel therapeutics aimed at various diseases, including cancer and neurological disorders, due to its ability to modulate biological pathways effectively.

In addition to its applications in drug discovery, Boc-(2R,3R)-3-amino-2-hydroxy-3-(3-methoxyphenyl)propionic acid serves as a valuable building block in organic synthesis, enabling the creation of complex molecules with enhanced pharmacological properties. Its favorable characteristics, such as high purity and excellent reactivity, make it a preferred choice among chemists and researchers seeking to innovate in medicinal chemistry. The compound's potential for customization and functionalization further underscores its significance in advancing pharmaceutical science.

CAS Number
1217672-32-6, 1391393-11-5
Purity
≥ 98 % (pureté chirale)
Molecular Formula
C 15 H 216
Molecular Weight
311.33
MDL Number
MFCD07363641
PubChem ID
53398456
Appearance
Solide blanc
Optical Rotation
[a] D 20 = -36,2 ± 2 ° (C = 0,5 dans le méthanol)
Conditions
Conserver entre 2 et 8 °C
General Information
CAS Number
1217672-32-6, 1391393-11-5
Purity
≥ 98 % (pureté chirale)
Molecular Formula
C 15 H 216
Molecular Weight
311.33
MDL Number
MFCD07363641
PubChem ID
53398456
Appearance
Solide blanc
Optical Rotation
[a] D 20 = -36,2 ± 2 ° (C = 0,5 dans le méthanol)
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-(3-methoxyphenyl)propionic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Peptide Synthesis: It is employed in the production of peptides, allowing for the incorporation of unique amino acid structures that can improve the stability and activity of therapeutic peptides.
  • Biochemical Research: Researchers use this compound to study enzyme interactions and metabolic pathways, providing insights into biological processes and potential therapeutic targets.
  • Material Science: The compound's properties make it useful in developing novel materials, particularly in creating polymers with enhanced mechanical and thermal stability.
  • Cosmetic Formulations: Its bioactive properties are leveraged in cosmetic products, offering benefits such as skin hydration and anti-aging effects, appealing to the growing demand for effective skincare solutions.

Citations