Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
33572
CAS Number:
1808268-53-2
N -Fmoc-7-méthyl-L-tryptophane
Purity:
≥ 99,5 % (HPLC chirale, HPLC)
Synonym(s):
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
Documents
$100.05 /25 mg
Taille
Request Bulk Quote
Product Information

N-Fmoc-7-methyl-L-tryptophan is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which allows for selective deprotection during the synthesis of peptides, making it an essential building block for researchers in the fields of medicinal chemistry and biochemistry. Its unique structure, characterized by the 7-methyl substitution on the indole ring, enhances its compatibility in various biochemical applications, including the design of bioactive peptides and the study of protein interactions.

This compound is particularly beneficial for researchers focusing on the development of pharmaceuticals targeting neurological disorders, as tryptophan derivatives are known precursors to serotonin and other neurotransmitters. Additionally, N-Fmoc-7-methyl-L-tryptophan can be employed in the synthesis of peptide-based therapeutics, offering improved stability and bioavailability compared to similar compounds. Its ability to facilitate complex peptide sequences makes it a valuable asset in both academic and industrial laboratories, ensuring efficient and effective research outcomes.

Synonyms
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
CAS Number
1808268-53-2
Purity
≥ 99,5 % (HPLC chirale, HPLC)
Molecular Formula
C27H24N2O4
Molecular Weight
440.49
MDL Number
MFCD31560627
PubChem ID
46737445
Appearance
Poudre blanche à blanc cassé ou rose clair
Optical Rotation
[a] 20 D = -20 ± 1 ° (C = 1 dans DMF)
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
CAS Number
1808268-53-2
Purity
≥ 99,5 % (HPLC chirale, HPLC)
Molecular Formula
C27H24N2O4
Molecular Weight
440.49
MDL Number
MFCD31560627
PubChem ID
46737445
Appearance
Poudre blanche à blanc cassé ou rose clair
Optical Rotation
[a] 20 D = -20 ± 1 ° (C = 1 dans DMF)
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

N-Fmoc-7-methyl-L-tryptophan 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, where its protective Fmoc group allows for selective deprotection and subsequent coupling reactions.
  • Drug Development: It plays a crucial role in the design of novel pharmaceuticals, especially in the development of compounds targeting serotonin receptors, which are important in treating mood disorders.
  • Biotechnology: Researchers use it in the production of modified proteins and enzymes, enhancing their stability and activity, which is vital for biocatalysis and therapeutic applications.
  • Research on Tryptophan Derivatives: This compound is instrumental in studying the biochemical pathways of tryptophan metabolism, aiding in understanding its role in various physiological processes.
  • Material Science: It is also explored in the development of advanced materials, particularly in creating functionalized polymers that can be used in drug delivery systems.

Citations