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Catalog Number:
15655
CAS Number:
329013-12-9
Boc-(R-3-amino-3-(3-hydroxyphenyl)propionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-D-β-Phe(3-OH)-OH, Boc-D-β-m-Tyr-OH
Documents
$65.40 /250MG
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Product Information

Boc-(R)-3-amino-3-(3-hydroxyphenyl)propionic acid is a versatile compound widely utilized in pharmaceutical and biochemical research. This amino acid derivative, characterized by its Boc (tert-butyloxycarbonyl) protecting group, is particularly valuable in peptide synthesis and drug development. Its unique structure allows for the incorporation of hydrophobic and hydrophilic properties, making it an ideal candidate for designing bioactive compounds. Researchers have leveraged this compound in the development of novel therapeutics, particularly in the fields of neuropharmacology and cancer research, where it can serve as a building block for more complex molecules.

The compound's ability to enhance solubility and stability in various formulations makes it a preferred choice for medicinal chemists. Its application extends to the synthesis of peptide-based drugs, where it can improve the pharmacokinetic profiles of the resulting compounds. Additionally, Boc-(R)-3-amino-3-(3-hydroxyphenyl)propionic acid is recognized for its potential in creating targeted delivery systems, thereby increasing the efficacy of therapeutic agents. This compound stands out due to its balance of functional groups, which can be tailored for specific applications, making it an essential tool for researchers and industry professionals alike.

Synonyms
Boc-D-β-Phe(3-OH)-OH, Boc-D-β-m-Tyr-OH
CAS Number
329013-12-9
Purity
≥ 98% (HPLC)
Molecular Formula
C14H19NO5
Molecular Weight
281.31
MDL Number
MFCD03427940
PubChem ID
2764539
Appearance
White to off-white Solid
Optical Rotation
[a]D25 = +38 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-D-β-Phe(3-OH)-OH, Boc-D-β-m-Tyr-OH
CAS Number
329013-12-9
Purity
≥ 98% (HPLC)
Molecular Formula
C14H19NO5
Molecular Weight
281.31
MDL Number
MFCD03427940
PubChem ID
2764539
Appearance
White to off-white Solid
Optical Rotation
[a]D25 = +38 ± 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-(3-hydroxyphenyl)propionic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders. Its unique structure allows for the development of drugs with improved efficacy and reduced side effects.
  • Peptide Synthesis: It is commonly used in solid-phase peptide synthesis, enhancing the stability and solubility of peptides. This application is crucial in producing therapeutic peptides that require precise amino acid sequences.
  • Bioconjugation: The compound can be employed in bioconjugation processes, linking biomolecules to create targeted drug delivery systems. This is particularly beneficial in cancer therapy, where targeted delivery can minimize damage to healthy cells.
  • Research in Neuroscience: Researchers utilize this compound to study the effects of amino acid derivatives on neurotransmitter systems, contributing to a better understanding of brain function and potential treatments for mental health disorders.
  • Cosmetic Formulations: Its antioxidant properties make it an attractive ingredient in cosmetic products aimed at skin protection and anti-aging, providing consumers with effective solutions for maintaining skin health.

Citations