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Catalog Number:
15650
CAS Number:
499995-78-7
Boc-(S)-3-amino-3-(2-hydroxyphenyl)propionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-L-β-Phe(2-OH)-OH, Boc-L-β-o-Tyr-OH
Documents
$72.31 /100MG
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Product Information

Boc-(S)-3-amino-3-(2-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, characterized by the presence of a 2-hydroxyphenyl group, contributes to its potential as a building block in the design of bioactive molecules, particularly in the development of inhibitors and modulators for various biological targets.

Researchers and industry professionals can leverage Boc-(S)-3-amino-3-(2-hydroxyphenyl)propionic acid in the synthesis of complex peptides and as a chiral auxiliary in asymmetric synthesis. Its application extends to the creation of novel therapeutic agents, particularly in the fields of oncology and neurology, where the modulation of specific biological pathways is crucial. The compound's favorable properties, including its ease of handling and compatibility with various coupling reagents, make it a valuable addition to any synthetic chemistry toolkit.

Synonyms
Boc-L-β-Phe(2-OH)-OH, Boc-L-β-o-Tyr-OH
CAS Number
499995-78-7
Purity
≥ 98% (HPLC)
Molecular Formula
C14H19NO5
Molecular Weight
281.31
MDL Number
MFCD03427901
PubChem ID
22309334
Melting Point
152 - 158 °C
Appearance
White powder
Optical Rotation
[a]D25 = -43 ± 2 º (C=1 in EtOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-β-Phe(2-OH)-OH, Boc-L-β-o-Tyr-OH
CAS Number
499995-78-7
Purity
≥ 98% (HPLC)
Molecular Formula
C14H19NO5
Molecular Weight
281.31
MDL Number
MFCD03427901
PubChem ID
22309334
Melting Point
152 - 158 °C
Appearance
White powder
Optical Rotation
[a]D25 = -43 ± 2 º (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-hydroxyphenyl)propionic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly in designing drugs that target specific biological pathways. Its unique structure allows for modifications that enhance drug efficacy.
  • Peptide Synthesis: It is commonly used in solid-phase peptide synthesis, where its protective Boc group facilitates the assembly of complex peptides while preventing unwanted reactions, ensuring high purity and yield.
  • Biochemical Research: Researchers employ this compound in studies related to enzyme activity and protein interactions, helping to elucidate mechanisms of action in biological systems.
  • Material Science: The compound can be incorporated into polymer matrices to create materials with specific properties, such as improved biocompatibility for medical devices or drug delivery systems.
  • Analytical Chemistry: It is utilized as a standard in chromatographic techniques, aiding in the quantification and analysis of related compounds in various samples, ensuring accuracy and reliability in research findings.

Citations