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Catalog Number:
15649
CAS Number:
500788-88-5
Boc-(R-3-amino-3-(2-hydroxyphenyl)propionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-D-β-Phe(2-OH)-OH, Boc-D-β-o-Tyr-OH
Documents
$58.39 /100MG
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Product Information

Boc-(R)-3-amino-3-(2-hydroxyphenyl)propionic acid is a versatile amino acid derivative that plays a crucial role in peptide synthesis and pharmaceutical research. This compound is particularly valued for its ability to serve as a building block in the development of bioactive peptides, which are essential in drug discovery and development. Its unique structure, featuring a Boc (tert-butyloxycarbonyl) protecting group, enhances its stability and solubility, making it an ideal candidate for various synthetic applications. Researchers utilize this compound in the synthesis of peptide analogs that can exhibit improved biological activity, thereby facilitating advancements in therapeutic agents.

In addition to its applications in peptide synthesis, Boc-(R)-3-amino-3-(2-hydroxyphenyl)propionic acid is also explored for its potential in the development of novel materials and as a chiral auxiliary in asymmetric synthesis. Its ability to provide chirality is particularly beneficial in the production of enantiomerically pure compounds, which are crucial in the pharmaceutical industry. This compound stands out due to its dual functionality, making it a valuable asset for both academic research and industrial applications.

Synonyms
Boc-D-β-Phe(2-OH)-OH, Boc-D-β-o-Tyr-OH
CAS Number
500788-88-5
Purity
≥ 99% (HPLC)
Molecular Formula
C14H19NO5
Molecular Weight
281.31
MDL Number
MFCD03427939
PubChem ID
22309334
Melting Point
159-165 °C
Appearance
Off-white powder
Optical Rotation
[a]D25 = +42 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-D-β-Phe(2-OH)-OH, Boc-D-β-o-Tyr-OH
CAS Number
500788-88-5
Purity
≥ 99% (HPLC)
Molecular Formula
C14H19NO5
Molecular Weight
281.31
MDL Number
MFCD03427939
PubChem ID
22309334
Melting Point
159-165 °C
Appearance
Off-white powder
Optical Rotation
[a]D25 = +42 ± 2º (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-(R)-3-amino-3-(2-hydroxyphenyl)propionic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important building block in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders due to its structural similarity to neurotransmitters.
  • Peptide Synthesis: It is frequently used in solid-phase peptide synthesis, allowing for the creation of complex peptides with enhanced stability and bioactivity, which is crucial in drug design.
  • Bioconjugation: The compound can be employed in bioconjugation processes, facilitating the attachment of drugs to antibodies or other biomolecules, thereby improving targeted drug delivery systems.
  • Research in Neuroscience: Its unique properties make it a valuable tool in neuroscience research, particularly in studying receptor interactions and signaling pathways, which can lead to new therapeutic strategies.
  • Cosmetic Formulations: Due to its antioxidant properties, it is also explored in cosmetic formulations aimed at skin protection and anti-aging, providing a dual benefit of enhancing skin health while offering functional benefits.

Citations