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Catalog Number:
31690
CAS Number:
77292-83-2
Boc-L-Pro-O-CH2-Ph-CH2-COOH
Purity:
≥ 97% (HPLC)
Documents
$43.87 /1G
Pack Size Availability Price
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Product Information

Boc-L-Pro-O-CH2-Ph-CH2-COOH is a versatile compound widely utilized in the field of organic synthesis and pharmaceutical research. This amino acid derivative features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an excellent choice for peptide synthesis and drug development. Its unique structure allows for the incorporation of phenyl and acetic acid functionalities, providing researchers with a valuable tool for creating complex molecules with specific biological activities.

In practical applications, Boc-L-Pro-O-CH2-Ph-CH2-COOH is particularly beneficial in the synthesis of bioactive peptides and pharmaceuticals, where precise control over molecular structure is crucial. Its ability to facilitate the formation of peptide bonds while maintaining stability under various reaction conditions makes it a preferred choice for chemists and researchers. Additionally, its compatibility with various coupling reagents and methods enhances its utility in diverse synthetic pathways, paving the way for innovative therapeutic solutions.

CAS Number
77292-83-2
Purity
≥ 97% (HPLC)
Molecular Formula
C19H25NO6
Molecular Weight
363.41
MDL Number
MFCD00273512
Melting Point
87-91 ?C
Appearance
White powder
Optical Rotation
[a]D20 = -33 ± 2° (C=0.5 in EtOH)
Conditions
Store at 0-8 °C
General Information
CAS Number
77292-83-2
Purity
≥ 97% (HPLC)
Molecular Formula
C19H25NO6
Molecular Weight
363.41
MDL Number
MFCD00273512
Melting Point
87-91 ?C
Appearance
White powder
Optical Rotation
[a]D20 = -33 ± 2° (C=0.5 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-L-Pro-O-CH2-Ph-CH2-COOH 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 used in pharmaceuticals.
  • Drug Development: Its structural properties make it valuable in the design of new drugs, particularly in developing compounds that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The compound can be used to create bioconjugates, which are essential in developing targeted therapies and diagnostics in the biomedical field, improving the precision of treatments.
  • Research in Neuroscience: It plays a role in studies related to neurotransmitter pathways, helping researchers understand brain functions and develop potential treatments for neurological disorders.
  • Cosmetic Formulations: Due to its stability and compatibility with various ingredients, it can be incorporated into cosmetic products, enhancing skin absorption and effectiveness of active ingredients.

Citations