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Catalog Number:
31692
Boc-L-Thr(Bzl)-O- CH2 -Ph-CH2 - COOH·DCHA
Purity:
≥ 99 % (HPLC)
Documents
$72.31 /1G
Taille
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Product Information

Boc-L-Thr(Bzl)-O-CH2-Ph-CH2-COOH·DCHA is a specialized amino acid derivative that plays a crucial role in peptide synthesis and pharmaceutical development. This compound features a unique structure that enhances its stability and solubility, making it an ideal choice for researchers and professionals in the fields of medicinal chemistry and biochemistry. Its benzyl and phenyl groups contribute to its hydrophobic characteristics, which can be advantageous in drug formulation and delivery systems.

The compound is particularly valuable in the synthesis of bioactive peptides, where it can serve as a building block due to its protective Boc (tert-butyloxycarbonyl) group, allowing for selective reactions. Additionally, its application extends to the development of targeted therapies and novel drug candidates, showcasing its potential in advancing therapeutic strategies. Researchers looking to optimize peptide sequences for improved efficacy will find this compound to be an essential tool in their arsenal, offering both versatility and reliability in various applications.

Purity
≥ 99 % (HPLC)
Molecular Formula
C 25 H 31 NO 7 · C 12 H 23 N
Molecular Weight
638.84
MDL Number
MFCD00273516
Melting Point
90-95 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -15 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
General Information
Purity
≥ 99 % (HPLC)
Molecular Formula
C 25 H 31 NO 7 · C 12 H 23 N
Molecular Weight
638.84
MDL Number
MFCD00273516
Melting Point
90-95 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -15 ± 2º (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-L-Thr(Bzl)-O-CH2-Ph-CH2-COOH·DCHA is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, which are essential in drug development and biochemistry. Its protective group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: The compound's unique structure can be modified to create novel therapeutic agents. Its application in medicinal chemistry helps researchers design drugs that target specific biological pathways.
  • Bioconjugation: It can be used in bioconjugation processes, linking biomolecules to other entities, such as drugs or imaging agents, which is crucial in targeted therapy and diagnostics.
  • Research in Neuroscience: Due to its potential to influence neurotransmitter systems, it is explored in neuroscience research for developing treatments for neurological disorders.
  • Cosmetic Formulations: The compound's properties make it suitable for use in cosmetic formulations, particularly in anti-aging products, where it can enhance skin penetration and efficacy of active ingredients.

Citations