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Catalog Number:
15620
CAS Number:
499995-74-3
Boc-(S-3-amino-3-(2-methylphenyl)propionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-D-β-Phe(2-Me)-OH, (S-Boc-2-methyl-β-phenylalanine
Documents
$106.96 /250MG
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Product Information

Boc-(S)-3-amino-3-(2-methylphenyl)propionic acid is a versatile amino acid derivative that plays a crucial role in the synthesis of peptide-based pharmaceuticals and biologically active compounds. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers in medicinal chemistry and drug development. Its unique structure allows for selective modifications, facilitating the creation of complex molecules with specific biological activities.

In the pharmaceutical industry, Boc-(S)-3-amino-3-(2-methylphenyl)propionic acid is utilized in the development of peptide therapeutics, particularly those targeting neurological disorders and metabolic diseases. Its ability to mimic natural amino acids while providing additional functional groups opens up new avenues for drug design. Researchers appreciate its ease of use in solid-phase peptide synthesis, where it aids in the efficient assembly of peptide chains. This compound stands out for its potential to enhance the efficacy and specificity of therapeutic agents, making it a valuable asset in modern drug discovery.

Synonyms
Boc-D-β-Phe(2-Me)-OH, (S-Boc-2-methyl-β-phenylalanine
CAS Number
499995-74-3
Purity
≥ 99% (HPLC)
Molecular Formula
C15H21NO4
Molecular Weight
279.34
MDL Number
MFCD03427895
PubChem ID
2764408
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-D-β-Phe(2-Me)-OH, (S-Boc-2-methyl-β-phenylalanine
CAS Number
499995-74-3
Purity
≥ 99% (HPLC)
Molecular Formula
C15H21NO4
Molecular Weight
279.34
MDL Number
MFCD03427895
PubChem ID
2764408
Appearance
White powder
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-3-(2-methylphenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the pharmaceutical industry, where it can enhance the stability and bioactivity of peptide drugs.
  • Drug Development: It plays a crucial role in the design of new therapeutic agents, especially in the development of drugs targeting neurological disorders, due to its structural properties that can influence receptor interactions.
  • Chiral Resolution: The compound is used in chiral resolution processes, helping researchers separate enantiomers in drug formulations, which is essential for ensuring the efficacy and safety of medications.
  • Bioconjugation: Its functional groups allow for effective bioconjugation, making it useful in creating targeted drug delivery systems that improve the precision of treatments in cancer therapy.
  • Research in Organic Chemistry: The compound is a key reagent in various organic synthesis reactions, enabling chemists to explore new pathways and develop innovative chemical processes.

Citations