Descubra el nuevo Chem-Impex: donde la innovación comienza con un vínculo.

Catalog Number:
04999
CAS Number:
204322-23-6
Ácido fmoc-L-1,2,3,4-tetrahidronorharman-3-carboxílico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-LTπ-OH, Fmoc-Tπ-OH
Documents
$39.26 /1G
Tamaño
Request Bulk Quote
Información del producto

Fmoc-L-1,2,3,4-tetrahydronorharman-3-carboxylic acid is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This compound features the Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure allows for efficient incorporation into various peptide sequences, making it an invaluable tool for researchers focused on developing novel therapeutics.

In addition to its role in peptide synthesis, Fmoc-L-1,2,3,4-tetrahydronorharman-3-carboxylic acid has shown potential in the development of bioactive molecules, particularly in the field of drug discovery. Its ability to facilitate the formation of complex structures can lead to the creation of compounds with enhanced biological activity. Researchers in pharmaceutical and biochemistry sectors will find this compound particularly beneficial for its ease of use and effectiveness in generating high-purity peptides, which are crucial for biological assays and therapeutic applications.

Número CAS
204322-23-6
Fórmula molecular
C27H22N2O4
Peso molecular
438.49
Número MDL
MFCD00673786
Rotación óptica
[a] 20 D = 55 ± 2 ° (C = 1 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
204322-23-6
Fórmula molecular
C27H22N2O4
Peso molecular
438.49
Número MDL
MFCD00673786
Rotación óptica
[a] 20 D = 55 ± 2 ° (C = 1 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
-
Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

Fmoc-L-1,2,3,4-tetrahydronorharman-3-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It is used in the design of novel pharmaceuticals, particularly in the development of compounds targeting neurological disorders, due to its structural similarity to biologically active molecules.
  • Bioconjugation: The chemical facilitates bioconjugation processes, enabling the attachment of biomolecules to therapeutic agents, which enhances drug delivery and efficacy.
  • Research in Neuroscience: Its unique structure makes it a valuable tool in neuroscience research, helping scientists explore the mechanisms of neuroactive compounds and their potential therapeutic effects.
  • Analytical Chemistry: The compound is employed in analytical methods to study interactions between biomolecules, providing insights into molecular behavior and aiding in the development of new analytical techniques.

Citas