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Catalog Number:
04083
CAS Number:
128779-47-5
Boc- p -phényl-D-phénylalanine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-D-Bip(4,4')-OH, Boc-D-Ala(4,4'-biphényl)-OH
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Product Information

Boc-p-phenyl-D-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers looking to streamline their synthesis processes. Its unique structure, characterized by the presence of two phenyl groups, allows for increased selectivity and specificity in various applications, including drug development and the creation of novel therapeutic agents.

In the realm of medicinal chemistry, Boc-p-phenyl-D-phenylalanine serves as a valuable building block for the synthesis of bioactive peptides. Its ability to mimic natural amino acids while providing enhanced properties makes it particularly advantageous in the design of peptide-based drugs. Researchers have successfully employed this compound in the development of targeted therapies, showcasing its potential in treating a range of diseases. With its favorable characteristics and practical applications, Boc-p-phenyl-D-phenylalanine stands out as a key component in advancing peptide chemistry and drug discovery.

Synonyms
Boc-D-Bip(4,4')-OH, Boc-D-Ala(4,4'-biphényl)-OH
CAS Number
128779-47-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C 20 H 234
Molecular Weight
341.4
MDL Number
MFCD00191185
PubChem ID
4623908
Melting Point
121-125? C
Optical Rotation
-38,50 ± 1º (c=1 dans EtOH)
Conditions
Conserver à 0-8°C
General Information
Synonyms
Boc-D-Bip(4,4')-OH, Boc-D-Ala(4,4'-biphényl)-OH
CAS Number
128779-47-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C 20 H 234
Molecular Weight
341.4
MDL Number
MFCD00191185
PubChem ID
4623908
Melting Point
121-125? C
Optical Rotation
-38,50 ± 1º (c=1 dans EtOH)
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-p-phenyl-D-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without affecting the overall structure. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: It plays a significant role in the design of new drugs, particularly in creating compounds that target specific receptors in the body, enhancing therapeutic efficacy and reducing side effects.
  • Biochemical Research: Researchers use it to study protein interactions and enzyme functions, providing insights into cellular processes and aiding in the development of novel biotechnological applications.
  • Material Science: The compound is applied in the creation of advanced materials, such as polymers and nanomaterials, which are essential in various industries, including electronics and healthcare.
  • Cosmetic Formulations: It is also explored in the cosmetic industry for its potential in formulating products that improve skin health, leveraging its biochemical properties to enhance product effectiveness.

Citations