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Catalog Number:
07289
CAS Number:
127095-97-0
Boc-Phe(3,4-diméthoxy)-OH
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-3,4-diméthoxy-L-phénylalanine, Boc-3,4-diméthoxy-Phe-OH, ( Acide S -Boc-2-amino-3-(3,4-diméthoxyphényl)propionique
Documents
$93.14 /250 mg
Taille
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Product Information

Boc-Phe(3,4-dimethoxy)-OH is a valuable compound widely utilized in peptide synthesis and pharmaceutical research. This amino acid derivative features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for various applications in organic synthesis. Its unique structure, characterized by the 3,4-dimethoxyphenyl group, allows for increased selectivity and efficiency in coupling reactions, which is crucial for the development of complex peptides and biologically active compounds. Researchers appreciate its role in facilitating the synthesis of peptide-based drugs, where precision and purity are paramount.

In addition to its applications in peptide synthesis, Boc-Phe(3,4-dimethoxy)-OH is also explored in the development of novel therapeutic agents and as a building block in medicinal chemistry. Its favorable properties, including high reactivity and compatibility with various coupling reagents, make it a preferred choice for chemists aiming to create innovative compounds with enhanced biological activity. This compound stands out for its ability to streamline synthesis processes while maintaining high yields and purity, making it an essential tool for professionals in the pharmaceutical and biotechnology sectors.

Synonyms
Boc-3,4-diméthoxy-L-phénylalanine, Boc-3,4-diméthoxy-Phe-OH, ( Acide S -Boc-2-amino-3-(3,4-diméthoxyphényl)propionique
CAS Number
127095-97-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 16 H 236
Molecular Weight
325.36
MDL Number
MFCD01317724
PubChem ID
22336961
Melting Point
102 - 104 °C
Appearance
Poudre blanc cassé
Optical Rotation
[a] 20 D = 22 ± 1 ° (C=1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Boc-3,4-diméthoxy-L-phénylalanine, Boc-3,4-diméthoxy-Phe-OH, ( Acide S -Boc-2-amino-3-(3,4-diméthoxyphényl)propionique
CAS Number
127095-97-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 16 H 236
Molecular Weight
325.36
MDL Number
MFCD01317724
PubChem ID
22336961
Melting Point
102 - 104 °C
Appearance
Poudre blanc cassé
Optical Rotation
[a] 20 D = 22 ± 1 ° (C=1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-Phe(3,4-dimethoxy)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing researchers to create complex structures efficiently.
  • Drug Development: Its unique structure aids in the design of new pharmaceuticals, especially in targeting specific biological pathways, enhancing the efficacy of drug candidates.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of biomolecules to drugs or imaging agents, which is crucial in developing targeted therapies.
  • Research in Neuroscience: It can be employed in studies related to neurotransmitter interactions, helping researchers understand the role of specific amino acids in brain function.
  • Analytical Chemistry: The compound is useful in developing analytical methods for detecting and quantifying biomolecules, providing essential data for various research applications.

Citations