Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
33651
Ácido Boc-(2 S ,3 S )-3-amino-2-hidroxi-3- m -tolil-propiónico
Purity:
≥ 98% (pureza quiral, RMN)
Documents
$100.05 /25 mg
Tamaño
Request Bulk Quote
Product Information

Boc-(2S,3S)-3-amino-2-hydroxy-3-m-tolyl-propionic acid is a versatile amino acid derivative that plays a crucial role in peptide synthesis and pharmaceutical research. This compound, often referred to as Boc-3-amino-2-hydroxy-3-m-tolylpropionic acid, features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and usability in various chemical reactions. Its unique structure allows for selective modifications, making it an invaluable building block in the development of bioactive peptides and drug candidates.

Researchers and industry professionals utilize Boc-(2S,3S)-3-amino-2-hydroxy-3-m-tolyl-propionic acid for its potential in creating novel therapeutic agents, particularly in the fields of medicinal chemistry and biotechnology. Its ability to facilitate the introduction of functional groups while maintaining compatibility with biological systems makes it a preferred choice for synthesizing complex molecules. Additionally, its favorable solubility and reactivity profile contribute to its effectiveness in various applications, including drug formulation and delivery systems.

Purity
≥ 98% (pureza quiral, RMN)
Molecular Formula
C 15 H 21 N º 5
Molecular Weight
295.33
MDL Number
MFCD07363620
Appearance
Sólido blanco
Optical Rotation
[a] D 20 = 40,4 ± 2 ° (C = 0,5 en MeOH)
Conditions
Conservar entre 2 y 8 °C.
General Information
Purity
≥ 98% (pureza quiral, RMN)
Molecular Formula
C 15 H 21 N º 5
Molecular Weight
295.33
MDL Number
MFCD07363620
Appearance
Sólido blanco
Optical Rotation
[a] D 20 = 40,4 ± 2 ° (C = 0,5 en MeOH)
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(2S,3S)-3-amino-2-hydroxy-3-m-tolyl-propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of pharmaceuticals targeting specific biological pathways.
  • Drug Development: It plays a crucial role in the design of new drugs, especially in the field of neuropharmacology, where modifications can enhance drug efficacy and selectivity.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents, improving their therapeutic and diagnostic capabilities.
  • Research in Enzyme Inhibition: It is valuable in studies aimed at understanding enzyme mechanisms and developing inhibitors, contributing to advancements in treating various diseases.
  • Material Science: The compound can be utilized in creating novel materials with specific properties, such as hydrophilicity or biocompatibility, beneficial for biomedical applications.

Citas