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Catalog Number:
00647
CAS Number:
54613-99-9
- Boc - - 2-chloro-ZL-lysine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-Lys(2-Cl-Z)-OH
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Product Information

La protection 2-Cl-Z est environ 50 fois plus stable que le groupe Z

Synonyms
Boc-L-Lys(2-Cl-Z)-OH
CAS Number
54613-99-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C19H27ClN2O6
Molecular Weight
414.89
MDL Number
MFCD00038386
PubChem ID
108253
Melting Point
65 - 80 ºC
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-L-Lys(2-Cl-Z)-OH
CAS Number
54613-99-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C19H27ClN2O6
Molecular Weight
414.89
MDL Number
MFCD00038386
PubChem ID
108253
Melting Point
65 - 80 ºC
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20
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

Na-Boc-Ne-2-chloro-Z-L-lysine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of pharmaceuticals. Its protective groups allow for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: It plays a significant role in the creation of novel therapeutic agents. By modifying the lysine residue, researchers can improve the pharmacological properties of drug candidates, leading to more effective treatments.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach drugs or imaging agents to biomolecules. This application is crucial in targeted drug delivery systems, enhancing the specificity and efficacy of treatments.
  • Research in Protein Engineering: It aids in the design of modified proteins with enhanced stability and activity. This is particularly beneficial in the fields of biotechnology and enzyme engineering, where tailored proteins can lead to innovative solutions.
  • Analytical Chemistry: The compound is utilized in analytical methods for studying amino acid sequences and modifications. Its unique structure allows for precise identification and quantification of peptides in complex mixtures.

Citations