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Catalog Number:
07105
CAS Number:
607366-20-1
Ácido N α - Fmoc- N β -(4,4-dimetil-2,6-dioxociclohex-1-ilideno)-3-metilbutil-L-2,3-diaminopropiónico
Purity:
≥ 98% (ensayo)
Synonym(s):
Fmoc-L-Dap(ivDde)-OH
Documents
$116.37 /250 mg
Tamaño
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Información del producto

Na-Fmoc-Nb-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-L-2,3-diaminopropionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amino acids during the synthesis of peptides. Its structural characteristics, including the 4,4-dimethyl-2,6-dioxocyclohex-1-ylidene moiety, enhance its stability and reactivity, making it an excellent choice for researchers focused on developing complex peptide structures.

In pharmaceutical research, this compound can serve as a building block for the synthesis of bioactive peptides, which are crucial in therapeutic applications, including cancer treatment and antimicrobial agents. Its ability to facilitate the formation of peptide bonds while maintaining high purity levels makes it a preferred choice among professionals in the field. Additionally, the compound's unique properties allow for improved yields and efficiency in peptide synthesis compared to traditional methods, making it a valuable asset in both academic and industrial laboratories.

Número CAS
607366-20-1
Fórmula molecular
C31H36N2O6
Peso molecular
532.5
Número MDL
MFCD01631659
Punto de fusión
152 - 165 ºC (Lit.)
Rotación óptica
[a] D 20 = 7 - 9 º (C=1 en MeOH)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
607366-20-1
Fórmula molecular
C31H36N2O6
Peso molecular
532.5
Número MDL
MFCD01631659
Punto de fusión
152 - 165 ºC (Lit.)
Rotación óptica
[a] D 20 = 7 - 9 º (C=1 en MeOH)
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
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Aplicaciones

Na-Fmoc-Nb-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-L-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without affecting others. This is crucial for creating complex peptides used in pharmaceuticals.
  • Drug Development: It plays a significant role in the development of new drugs, particularly in designing peptides that can target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the delivery and effectiveness of drugs.
  • Research in Oncology: It is applied in cancer research for developing peptide-based therapies that can selectively target and destroy cancer cells, offering a promising alternative to traditional treatments.
  • Material Science: This chemical is also explored in the development of new materials with specific properties, such as enhanced biocompatibility for medical devices.

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