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Catalog Number:
24643
CAS Number:
1393687-43-8
Fmoc-D-Lys(2-Cl-Z)-OH
Purity:
≥ 98%
Synonym(s):
Fmoc-Ne-2-chloro-Z-D-lysine
Documents
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Product Information

Fmoc-D-Lys(2-Cl-Z)-OH is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which is essential for the selective protection of amino groups during solid-phase peptide synthesis. Its unique structure, characterized by the presence of a 2-chlorophenyl substituent, enhances its reactivity and specificity, making it an ideal choice for researchers aiming to develop complex peptides with high purity and yield.

In the pharmaceutical industry, Fmoc-D-Lys(2-Cl-Z)-OH plays a crucial role in the design of peptide-based therapeutics, particularly in the development of targeted drug delivery systems and biologically active compounds. Its ability to facilitate the introduction of lysine residues into peptide chains allows for the incorporation of functional groups that can enhance solubility, stability, and bioactivity. Researchers and industry professionals can leverage this compound to create innovative solutions in drug formulation and therapeutic applications, making it a valuable addition to any laboratory focused on peptide chemistry.

Synonyms
Fmoc-Ne-2-chloro-Z-D-lysine
CAS Number
1393687-43-8
Purity
≥ 98%
Molecular Formula
C29H29N2O6Cl
Molecular Weight
536.99
MDL Number
MFCD01861352
PubChem ID
4169191
Melting Point
112-117 ?C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = +8.9 ± 2º (C=1 in DMF)
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-Ne-2-chloro-Z-D-lysine
CAS Number
1393687-43-8
Purity
≥ 98%
Molecular Formula
C29H29N2O6Cl
Molecular Weight
536.99
MDL Number
MFCD01861352
PubChem ID
4169191
Melting Point
112-117 ?C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = +8.9 ± 2º (C=1 in DMF)
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

Fmoc-D-Lys(2-Cl-Z)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as an essential building block in the synthesis of peptides, allowing researchers to create complex structures for various biological studies.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, particularly in targeting specific receptors due to its selective reactivity.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules to enhance drug delivery systems and improve therapeutic efficacy.
  • Research in Cancer Treatment: It plays a role in the development of targeted therapies, where modifications can lead to more effective treatments with fewer side effects.
  • Diagnostic Applications: Fmoc-D-Lys(2-Cl-Z)-OH is also explored in diagnostic tools, aiding in the detection of specific biomolecules in clinical settings.

Citations