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Catalog Number:
16177
CAS Number:
235788-61-1
Acide N α -Fmoc- N γ -(4,4-diméthyl-2,6-dioxocyclohex-1-ylidène)éthyl-L-2,4-diaminobutyrique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Dab(Dde)-OH
Documents
$72.31 /100 mg
Taille
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Product Information

Na-Fmoc-Ng-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl-L-2,4-diaminobutyric acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound, often referred to as Fmoc-protected amino acid, serves as a crucial building block in the synthesis of peptides and proteins, enabling researchers to create complex biomolecules with precision. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, allows for selective deprotection under mild conditions, making it an ideal choice for chemists focused on developing novel therapeutics.

In addition to its role in peptide synthesis, this compound has shown potential in various applications, including the development of enzyme inhibitors and targeted drug delivery systems. Its stability and compatibility with a range of coupling reagents enhance its utility in organic synthesis. Researchers in medicinal chemistry and biochemistry will find this compound particularly valuable for advancing their projects, as it facilitates the efficient construction of bioactive molecules while minimizing side reactions.

Synonyms
Fmoc-L-Dab(Dde)-OH
CAS Number
235788-61-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C29H32N2O6
Molecular Weight
504.6
MDL Number
MFCD11111552
PubChem ID
137317221
Melting Point
137 - 155 °C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] 20 D 3 )
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-L-Dab(Dde)-OH
CAS Number
235788-61-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C29H32N2O6
Molecular Weight
504.6
MDL Number
MFCD11111552
PubChem ID
137317221
Melting Point
137 - 155 °C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] 20 D 3 )
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Na-Fmoc-Ng-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl-L-2,4-diaminobutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing for the selective modification of amino acids. Its stability under various conditions makes it ideal for complex peptide chains.
  • Drug Development: It plays a crucial role in the design of novel therapeutic agents, particularly in the development of peptide-based drugs that can target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation techniques, enabling the attachment of biomolecules to drugs or imaging agents, enhancing their efficacy and targeting capabilities.
  • Research in Cancer Therapy: Its unique structure allows researchers to explore new avenues in cancer treatment by designing peptides that can inhibit tumor growth or enhance immune response.
  • Material Science: The compound is also explored in the development of advanced materials, particularly in creating polymers that respond to biological stimuli, which can be used in drug delivery systems.

Citations