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Catalog Number:
03210
CAS Number:
66605-57-0
Boc-L-phenylalaninol
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-Phe-ol
Documents
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Product Information

Boc-L-phenylalaninol is a versatile amino alcohol widely utilized in the synthesis of various pharmaceutical compounds and peptides. This compound features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and reactivity in organic synthesis. Its unique structure allows for the selective introduction of functional groups, making it an essential building block in the development of biologically active molecules. Researchers and industry professionals appreciate its role in asymmetric synthesis, particularly in the production of chiral intermediates and drug candidates.

The compound's ability to facilitate the formation of peptide bonds and its compatibility with various coupling reagents make it a preferred choice in peptide synthesis. Additionally, Boc-L-phenylalaninol is employed in the preparation of prodrugs and other derivatives, expanding its application in medicinal chemistry. With its favorable properties and significant utility, this compound stands out as a key ingredient in the pharmaceutical and biotechnology sectors, driving innovation and enhancing the efficiency of drug development processes.

Synonyms
Boc-L-Phe-ol
CAS Number
66605-57-0
Purity
≥ 99% (HPLC)
Molecular Formula
C14H21NO3
Molecular Weight
251.31
MDL Number
MFCD00076976
PubChem ID
545866
Melting Point
93-100 °C
Appearance
White powder
Optical Rotation
[a]D25 = -27 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-Phe-ol
CAS Number
66605-57-0
Purity
≥ 99% (HPLC)
Molecular Formula
C14H21NO3
Molecular Weight
251.31
MDL Number
MFCD00076976
PubChem ID
545866
Melting Point
93-100 °C
Appearance
White powder
Optical Rotation
[a]D25 = -27 ± 2º (C=1 in MeOH)
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-L-phenylalaninol is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing chemists to selectively modify amino acids without affecting others. This is crucial for creating complex peptides with desired biological activities.
  • Drug Development: It plays a significant role in the pharmaceutical industry, particularly in the design of new drugs that target specific biological pathways. Its unique structure can enhance the efficacy of drug candidates.
  • Chiral Catalysis: The compound is used in asymmetric synthesis, where it helps produce chiral molecules that are important in various applications, including the creation of fine chemicals and agrochemicals.
  • Bioconjugation: Boc-L-phenylalaninol is utilized in bioconjugation processes, linking biomolecules to therapeutic agents, which can improve the specificity and effectiveness of treatments in targeted therapies.
  • Research in Neuroscience: Its derivatives are explored in studies related to neurotransmitter systems, contributing to the understanding of neuropharmacology and the development of potential treatments for neurological disorders.

Citations