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Catalog Number:
05130
CAS Number:
55533-25-0
Boc-L-Phe(4-NHZ)-OH·DCHA
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-4-(Z-amino)-L-phenylalanine dicyclohexylammonium salt
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Product Information

Boc-L-Phe(4-NHZ)-OH·DCHA is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This protected amino acid derivative features a Boc (tert-butyloxycarbonyl) group, enhancing its stability and solubility, making it an ideal choice for researchers focusing on the development of peptide-based therapeutics. Its unique structure allows for selective reactions, facilitating the incorporation of the 4-amino group into peptides, which can be crucial for creating bioactive compounds with specific functionalities.

In the field of medicinal chemistry, Boc-L-Phe(4-NHZ)-OH·DCHA serves as a valuable building block for the synthesis of peptide hormones, enzyme inhibitors, and other biologically active molecules. Its ability to enhance the pharmacokinetic properties of peptides makes it a preferred choice among researchers aiming to optimize drug design. Additionally, its compatibility with various coupling reagents and reaction conditions further broadens its applicability in synthetic organic chemistry, ensuring that it meets the diverse needs of professionals in the industry.

Synonyms
Boc-4-(Z-amino)-L-phenylalanine dicyclohexylammonium salt
CAS Number
55533-25-0
Purity
≥ 99% (HPLC)
Molecular Formula
C22H26N2O6·C12H23N
Molecular Weight
595.7
MDL Number
MFCD08236868
PubChem ID
4712501
Melting Point
150-155 °C
Appearance
White powder
Optical Rotation
[a]D20 = +33 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-4-(Z-amino)-L-phenylalanine dicyclohexylammonium salt
CAS Number
55533-25-0
Purity
≥ 99% (HPLC)
Molecular Formula
C22H26N2O6·C12H23N
Molecular Weight
595.7
MDL Number
MFCD08236868
PubChem ID
4712501
Melting Point
150-155 °C
Appearance
White powder
Optical Rotation
[a]D20 = +33 ± 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-Phe(4-NHZ)-OH·DCHA is widely utilized in research focused on

  • Peptide Synthesis: This compound is an important building block in the synthesis of peptides, particularly for creating modified amino acids that enhance the stability and bioactivity of therapeutic peptides.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for developing new drugs, especially in designing inhibitors that can target specific proteins in diseases.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and targeted drug delivery systems.
  • Research in Cancer Therapeutics: It is utilized in the development of cancer therapies, where modified peptides can improve the selectivity and efficacy of treatments against tumor cells.
  • Antibody Production: This compound aids in the production of antibodies by modifying antigens, enhancing the immune response for better diagnostic and therapeutic outcomes.

Citations