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Catalog Number:
15656
CAS Number:
499995-79-8
Boc-(S-3-amino-3-(3-hydroxyphenyl)propionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-L-β-Phe(3-OH)-OH, Boc-L-β-m-Tyr-OH
Documents
$72.31 /100MG
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Product Information

Boc-(S)-3-amino-3-(3-hydroxyphenyl)propionic acid is a versatile compound widely utilized in pharmaceutical and biochemical research. 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 development. Its unique structure allows for the incorporation of hydrophobic and hydrophilic properties, facilitating the design of novel therapeutic agents. Researchers have found it particularly useful in the synthesis of bioactive peptides and as a building block in the development of enzyme inhibitors and receptor ligands.

The compound's potential applications extend to the fields of medicinal chemistry and materials science, where it can be employed in the creation of targeted drug delivery systems and functionalized polymers. Its ability to mimic natural amino acids while providing additional functional groups makes it a valuable tool for scientists aiming to innovate in drug design and biomaterials. With its favorable properties and diverse applications, Boc-(S)-3-amino-3-(3-hydroxyphenyl)propionic acid stands out as a significant asset for researchers and industry professionals alike.

Synonyms
Boc-L-β-Phe(3-OH)-OH, Boc-L-β-m-Tyr-OH
CAS Number
499995-79-8
Purity
≥ 98% (HPLC)
Molecular Formula
C14H19NO5
Molecular Weight
281.31
MDL Number
MFCD03427902
PubChem ID
2764541
Appearance
White powder
Optical Rotation
[a]D25 = -43 ± 3º (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-β-Phe(3-OH)-OH, Boc-L-β-m-Tyr-OH
CAS Number
499995-79-8
Purity
≥ 98% (HPLC)
Molecular Formula
C14H19NO5
Molecular Weight
281.31
MDL Number
MFCD03427902
PubChem ID
2764541
Appearance
White powder
Optical Rotation
[a]D25 = -43 ± 3º (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-(3-hydroxyphenyl)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 bioactive peptides that can be used in pharmaceuticals.
  • Drug Development: Its unique structure allows for the design of novel drugs targeting specific biological pathways, making it valuable in the pharmaceutical industry for creating new therapeutic agents.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules to enhance drug delivery systems, which is crucial in improving the efficacy of treatments.
  • Research in Neuroscience: Given its structural properties, it is employed in studies related to neurotransmitter systems, aiding in the understanding of neurological disorders.
  • Material Science: It can also be used in the development of functional materials, such as hydrogels, which have applications in drug delivery and tissue engineering.

Citations