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

Catalog Number:
16683
CAS Number:
59937-41-6
Ácido Boc-(2 S ,3 S )-3-amino-2-hidroxi-3-fenilpropiónico
Purity:
≥ 97 % (HPLC)
Documents
$148.22 /25 mg
Tamaño
Request Bulk Quote
Product Information

Boc-(2S,3S)-3-amino-2-hydroxy-3-phenylpropionic acid is a versatile amino acid derivative that plays a crucial role in peptide synthesis and pharmaceutical development. This compound is particularly valued for its ability to serve as a protective group in the synthesis of complex peptides, allowing for selective reactions and enhancing the stability of intermediates. Its unique structure, featuring a Boc (tert-butyloxycarbonyl) protecting group, facilitates the introduction of various functional groups, making it an essential building block in the design of bioactive molecules.

Researchers and industry professionals utilize Boc-(2S,3S)-3-amino-2-hydroxy-3-phenylpropionic acid in the development of therapeutic peptides and drug candidates, particularly in the fields of oncology and neurology. Its compatibility with various coupling reagents and its ability to undergo selective deprotection make it an ideal choice for complex synthetic pathways. The compound's stability and ease of handling further enhance its appeal, ensuring that it meets the rigorous demands of modern chemical research and development.

CAS Number
59937-41-6
Purity
≥ 97 % (HPLC)
Molecular Formula
C 14 H 19 N.º 5
Molecular Weight
281.3
MDL Number
MFCD07363511
PubChem ID
21254115
Melting Point
94 - 100 ?C
Appearance
Polvo blanco
Optical Rotation
[a] D 25 = +42 ± 2 º (C=1 en EtOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
59937-41-6
Purity
≥ 97 % (HPLC)
Molecular Formula
C 14 H 19 N.º 5
Molecular Weight
281.3
MDL Number
MFCD07363511
PubChem ID
21254115
Melting Point
94 - 100 ?C
Appearance
Polvo blanco
Optical Rotation
[a] D 25 = +42 ± 2 º (C=1 en EtOH)
Conditions
Conservar entre 0 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-phenylpropionic 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 pharmaceutical industry, where it helps create biologically active compounds.
  • Drug Development: It plays a crucial role in the development of new drugs, especially those targeting neurological disorders, due to its ability to modify amino acid sequences effectively.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach drugs or imaging agents to proteins, enhancing therapeutic efficacy and diagnostic capabilities.
  • Research in Enzyme Inhibition: It is valuable in studies aimed at understanding enzyme mechanisms, particularly in the context of developing inhibitors for specific enzymes involved in disease pathways.
  • Cosmetic Formulations: The compound finds application in cosmetic products, where it can contribute to skin health by acting as a moisturizing agent and promoting skin repair.

Citas