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

Catalog Number:
02676
CAS Number:
428868-52-4
Fmoc-N-methyl-O-benzyl-L-tyrosine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-N-Me-L-Tyr(Bzl)-OH
Documents
$103.56 /250MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Fmoc-N-methyl-O-benzyl-L-tyrosine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which is essential for the selective protection of the amino group during the synthesis of complex peptides. Its unique structure, incorporating a methyl and benzyl group, enhances its solubility and stability, making it an ideal choice for researchers focused on developing high-purity peptides for pharmaceutical applications.

In the field of medicinal chemistry, Fmoc-N-methyl-O-benzyl-L-tyrosine serves as a crucial building block in the synthesis of bioactive peptides, which can be used in various therapeutic areas, including cancer treatment and hormone regulation. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of the amino acid structure allows for the creation of tailored peptides with specific biological activities. This compound stands out for its ease of use and efficiency in peptide coupling reactions, making it a preferred choice among professionals in the pharmaceutical and biotechnology industries.

Synonyms
Fmoc-N-Me-L-Tyr(Bzl)-OH
CAS Number
428868-52-4
Purity
≥ 98% (HPLC)
Molecular Formula
C32H29NO5
Molecular Weight
507.6
MDL Number
MFCD00270746
PubChem ID
73090543
Melting Point
63-69 ºC
Optical Rotation
[a]D = - 38 ± 2 º (C=1 in acetone)
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-N-Me-L-Tyr(Bzl)-OH
CAS Number
428868-52-4
Purity
≥ 98% (HPLC)
Molecular Formula
C32H29NO5
Molecular Weight
507.6
MDL Number
MFCD00270746
PubChem ID
73090543
Melting Point
63-69 ºC
Optical Rotation
[a]D = - 38 ± 2 º (C=1 in acetone)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-N-methyl-O-benzyl-L-tyrosine 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 (SPPS), allowing for the creation of complex peptide sequences with high purity.
  • Drug Development: Its unique structure makes it valuable in the pharmaceutical industry for developing new drugs, especially those targeting specific receptors or enzymes, enhancing therapeutic efficacy.
  • Bioconjugation: The compound is used in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Research in Neuroscience: Fmoc-N-methyl-O-benzyl-L-tyrosine is employed in studies related to neurotransmitter systems, aiding in the understanding of neurological pathways and the development of neuroactive compounds.
  • Protein Engineering: This chemical is instrumental in modifying proteins to enhance their stability and functionality, which is crucial in various biotechnological applications, including enzyme engineering and antibody production.

Citations