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Catalog Number:
33633
CAS Number:
129786-68-1
Boc-α-metil-L-alilglicina
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$100.05 /25 mg
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Product Information

Boc-a-methyl-L-allylglycine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and medicinal chemistry. This compound is particularly valued for its protective Boc (tert-butyloxycarbonyl) group, which facilitates the selective functionalization of amino acids during synthetic processes. Its unique structure allows for the introduction of the allyl group, making it an essential building block in the development of bioactive peptides and pharmaceuticals. Researchers utilize Boc-a-methyl-L-allylglycine in the synthesis of peptide-based drugs, where its stability and reactivity can enhance the efficacy of therapeutic agents.

In addition to its applications in drug development, this compound is also employed in the study of enzyme mechanisms and protein interactions, providing insights into biological processes. Its ability to serve as a chiral auxiliary further expands its utility in asymmetric synthesis, making it a valuable asset for chemists seeking to create enantiomerically pure compounds. With its broad range of applications and significant advantages in peptide synthesis, Boc-a-methyl-L-allylglycine is an indispensable tool for researchers and industry professionals alike.

CAS Number
129786-68-1
Molecular Formula
Boc-α-metil-L-alilglicina
Molecular Weight
229.27
MDL Number
MFCD02682443
PubChem ID
53398095
Conditions
Conservar entre 2 y 8 °C.
General Information
CAS Number
129786-68-1
Molecular Formula
Boc-α-metil-L-alilglicina
Molecular Weight
229.27
MDL Number
MFCD02682443
PubChem ID
53398095
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-a-methyl-L-allylglycine 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 biologically active compounds. Its protective Boc group allows for selective reactions, enhancing efficiency in complex synthesis.
  • Drug Development: Researchers leverage Boc-a-methyl-L-allylglycine in the design of novel pharmaceuticals. Its unique structure can lead to the creation of compounds with improved bioactivity and selectivity, addressing specific therapeutic targets.
  • Bioconjugation: This chemical is used in bioconjugation processes, where it can be attached to biomolecules to create targeted drug delivery systems. This application is crucial in developing therapies that minimize side effects while maximizing efficacy.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, as derivatives can mimic natural compounds, aiding in the exploration of neurological pathways and potential treatments for neurodegenerative diseases.
  • Analytical Chemistry: Boc-a-methyl-L-allylglycine is employed in analytical methods to quantify amino acids and peptides in various samples, providing essential data for quality control in pharmaceutical manufacturing.

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