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

Catalog Number:
16878
CAS Number:
1175919-93-3
Boc-O-allyl-L-m-tyrosine
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-m-Tyr(All)-OH, Boc-L-3-Allyloxyphenylalanine, Boc-m-Tyr(All)-OH
Documents
$127.79 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-O-allyl-L-m-tyrosine is a versatile amino acid derivative that plays a significant role in peptide synthesis and pharmaceutical research. This compound is particularly valued for its unique protective Boc (tert-butyloxycarbonyl) group, which facilitates the selective modification of amino acids during the synthesis of complex peptides. Its allyl group enhances reactivity, making it an excellent choice for applications in organic synthesis and medicinal chemistry. Researchers utilize Boc-O-allyl-L-m-tyrosine in the development of novel therapeutic agents, especially in the field of cancer research, where it can be incorporated into peptide-based drugs to improve efficacy and specificity.

In addition to its applications in drug development, Boc-O-allyl-L-m-tyrosine is also used in the synthesis of bioactive compounds and as a building block in the preparation of various functionalized peptides. Its favorable properties, such as stability under a range of conditions and compatibility with various coupling reagents, make it a preferred choice for chemists looking to streamline their synthetic processes. With its potential to enhance the bioactivity of peptides, Boc-O-allyl-L-m-tyrosine stands out as a valuable tool for researchers and industry professionals alike.

Synonyms
Boc-L-m-Tyr(All)-OH, Boc-L-3-Allyloxyphenylalanine, Boc-m-Tyr(All)-OH
CAS Number
1175919-93-3
Purity
≥ 99% (HPLC)
Molecular Formula
C17H23NO5
Molecular Weight
321.37
MDL Number
MFCD08061618
PubChem ID
11163013
Appearance
White to off-white powder
Optical Rotation
[a]D25 = +33.0 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-m-Tyr(All)-OH, Boc-L-3-Allyloxyphenylalanine, Boc-m-Tyr(All)-OH
CAS Number
1175919-93-3
Purity
≥ 99% (HPLC)
Molecular Formula
C17H23NO5
Molecular Weight
321.37
MDL Number
MFCD08061618
PubChem ID
11163013
Appearance
White to off-white powder
Optical Rotation
[a]D25 = +33.0 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-O-allyl-L-m-tyrosine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of therapeutic agents. Its protective Boc group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In pharmaceutical research, it is used to create novel compounds that can target specific biological pathways. Its unique structure aids in the design of drugs with improved efficacy and reduced side effects.
  • Bioconjugation: The compound is employed in bioconjugation processes, where it can be linked to biomolecules like proteins or antibodies. This application is crucial in developing targeted therapies and diagnostic tools.
  • Research in Neuroscience: Due to its structural similarity to neurotransmitters, it is used in studies investigating neurological pathways and potential treatments for neurodegenerative diseases.
  • Material Science: The compound finds applications in creating functionalized materials, enhancing properties such as solubility and reactivity, which are important in developing advanced materials for various industrial applications.

Citations