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Catalog Number:
15634
CAS Number:
499995-76-5
Boc-(S-3-amino-3-(2-methoxyphenyl)propionic acid
Purity:
≥ 97% (Assay)
Synonym(s):
Boc-L-β-Phe(2-OMe)-OH, (S-Boc-2-methoxy-β-phenylalanine
Documents
$72.31 /250MG
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Product Information

Boc-(S)-3-amino-3-(2-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 allows for selective modifications, facilitating the design of bioactive compounds with improved efficacy and reduced side effects.

Researchers and industry professionals can leverage this compound in the synthesis of novel therapeutic agents, particularly in the fields of neuropharmacology and medicinal chemistry. Its application extends to the development of inhibitors and modulators that target specific biological pathways, showcasing its potential in creating innovative treatments for various diseases. The compound's favorable properties, including its ability to enhance the bioavailability of active pharmaceutical ingredients, make it a valuable asset in drug discovery and development processes.

Synonyms
Boc-L-β-Phe(2-OMe)-OH, (S-Boc-2-methoxy-β-phenylalanine
CAS Number
499995-76-5
Purity
≥ 97% (Assay)
Molecular Formula
C15H21NO5
Molecular Weight
295.33
MDL Number
MFCD03427898
PubChem ID
44630853
Appearance
White to off-white solid
Optical Rotation
[a]D25 = -28.5° to -35.5º (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-β-Phe(2-OMe)-OH, (S-Boc-2-methoxy-β-phenylalanine
CAS Number
499995-76-5
Purity
≥ 97% (Assay)
Molecular Formula
C15H21NO5
Molecular Weight
295.33
MDL Number
MFCD03427898
PubChem ID
44630853
Appearance
White to off-white solid
Optical Rotation
[a]D25 = -28.5° to -35.5º (C=1 in EtOH)
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-methoxyphenyl)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 development of new therapeutic agents, especially in the field of neuropharmacology, due to its ability to mimic natural amino acids.
  • Research in Neuroscience: The compound is used in studies investigating neurotransmitter systems, helping researchers understand the mechanisms of action for various neurological disorders.
  • Bioconjugation: Its reactive functional groups allow for effective bioconjugation processes, which are essential in creating targeted drug delivery systems and diagnostic tools.
  • Chiral Resolution: The compound is instrumental in chiral resolution techniques, aiding in the separation of enantiomers in complex mixtures, which is vital for producing optically pure substances in pharmaceuticals.

Citations