Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
22739
Acide (S)-Boc-2-amino-6-benzyloxy-hexanoïque·DCHA
Purity:
≥ 97 % (HPLC)
Documents
$113.87 /100 mg
Taille
Request Bulk Quote
Product Information

(S)-Boc-2-amino-6-benzyloxy-hexanoic acid·DCHA is a versatile compound widely utilized in the field of organic synthesis and pharmaceutical research. This compound, also known as (S)-Boc-2-amino-6-benzyloxyhexanoic acid, features a Boc (tert-butyloxycarbonyl) protecting group, which is crucial for the selective protection of amines during peptide synthesis. Its unique structure allows for the introduction of a benzyloxy group, enhancing its reactivity and making it an ideal candidate for various coupling reactions in the development of bioactive molecules.

Researchers and industry professionals can leverage (S)-Boc-2-amino-6-benzyloxy-hexanoic acid·DCHA in the synthesis of peptide-based therapeutics, where its ability to facilitate the formation of peptide bonds is invaluable. Additionally, its application in drug discovery and development processes highlights its significance in creating complex molecular architectures. The compound's stability and ease of handling further enhance its appeal, making it a preferred choice for laboratories focused on innovative drug design and synthesis.

Purity
≥ 97 % (HPLC)
Molecular Formula
C 18 H 27 NO 5 · C 12 H 23 N
Molecular Weight
518.74
MDL Number
MFCD09952620
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = +11,9 ± 1º (C=1 dans MeOH)
Conditions
Conserver à 0-8 °C
General Information
Purity
≥ 97 % (HPLC)
Molecular Formula
C 18 H 27 NO 5 · C 12 H 23 N
Molecular Weight
518.74
MDL Number
MFCD09952620
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = +11,9 ± 1º (C=1 dans MeOH)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(S)-Boc-2-amino-6-benzyloxy-hexanoic acid·DCHA is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, which are vital for developing new drugs and therapeutic agents.
  • Drug Development: Its unique structure allows for modifications that enhance the bioavailability and efficacy of pharmaceutical compounds, making it valuable in medicinal chemistry.
  • Bioconjugation: The presence of the benzyloxy group facilitates bioconjugation processes, which are essential for creating targeted drug delivery systems in cancer therapy.
  • Research in Neuroscience: This compound can be used in the development of neuroprotective agents, contributing to studies aimed at treating neurodegenerative diseases.
  • Cosmetic Formulations: Its properties make it suitable for use in cosmetic products, particularly those aiming to enhance skin hydration and elasticity.

Citations