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Catalog Number:
37072
CAS Number:
1446752-60-8
Nα - (4,4-Dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-Nε-Fmoc-L-lysine
Purity:
≥ 99% (HPLC)
Synonym(s):
ivDde-L-Lys(Fmoc)-OH
Documents
$80.00 /100MG
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Product Information

Na - (4,4-Dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-Ne-Fmoc-L-lysine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a unique structure that enhances its stability and solubility, making it an excellent choice for researchers focused on creating complex peptides with improved bioactivity. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into solid-phase peptide synthesis, streamlining the process for chemists and biochemists alike.

This compound is particularly valuable in the pharmaceutical industry for the development of peptide-based therapeutics, where precise modifications can significantly impact efficacy and safety profiles. Additionally, its distinctive cyclohexenylidene moiety can impart unique biological properties, potentially leading to novel therapeutic applications. Researchers can leverage this compound to explore new avenues in drug discovery, particularly in the fields of oncology and immunology, where tailored peptides are increasingly important.

Synonyms
ivDde-L-Lys(Fmoc)-OH
CAS Number
1446752-60-8
Purity
≥ 99% (HPLC)
Molecular Formula
C34H42N2O6
Molecular Weight
574.7
MDL Number
MFCD27957348
PubChem ID
155896872
Melting Point
93 - 96 ?C (Lit.)
Appearance
White crystalline powder
Optical Rotation
[a]D20 = 11 ± 2 ° (C=1 in CHCl3)
Conditions
Store at 2 - 8 °C
General Information
Synonyms
ivDde-L-Lys(Fmoc)-OH
CAS Number
1446752-60-8
Purity
≥ 99% (HPLC)
Molecular Formula
C34H42N2O6
Molecular Weight
574.7
MDL Number
MFCD27957348
PubChem ID
155896872
Melting Point
93 - 96 ?C (Lit.)
Appearance
White crystalline powder
Optical Rotation
[a]D20 = 11 ± 2 ° (C=1 in CHCl3)
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na - (4,4-Dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-Ne-Fmoc-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 solid-phase peptide synthesis, enhancing the efficiency and yield of desired peptides.
  • Drug Development: It plays a crucial role in the development of pharmaceuticals, especially in creating targeted therapies that require specific peptide sequences for effective treatment.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Research in Protein Engineering: It aids in the modification of proteins, enabling scientists to study protein interactions and functions, which is vital in understanding biological processes.
  • Cosmetic Formulations: The compound is also explored in cosmetic chemistry for its potential in formulating products that require specific peptide-based ingredients for enhanced skin benefits.

Citations