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Catalog Number:
12856
CAS Number:
114873-06-2
Boc-3-metil-L-fenilalanina
Purity:
≥ 99,0 % (HPLC)
Synonym(s):
Boc-L-Fe(3-Me)-OH, Boc- m -Me-L-Phe-OH, Boc-Fe(3-Me)-OH
Documents
$51.18 /1G
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Product Information

Boc-3-methyl-L-phenylalanine is a valuable amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butyloxycarbonyl (Boc) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers working on complex peptide sequences. Its unique structure, characterized by a 3-methylphenyl side chain, allows for increased hydrophobic interactions, which can be advantageous in the development of bioactive peptides and drug candidates.

In the pharmaceutical industry, Boc-3-methyl-L-phenylalanine serves as a crucial building block in the synthesis of various therapeutic peptides, including those targeting neurological disorders and cancer. Its ability to improve the pharmacokinetic properties of peptides makes it a preferred choice among researchers looking to optimize drug formulations. Additionally, this compound's compatibility with various coupling reagents and methods further enhances its utility in peptide chemistry, ensuring that it meets the diverse needs of professionals in the field.

Synonyms
Boc-L-Fe(3-Me)-OH, Boc- m -Me-L-Phe-OH, Boc-Fe(3-Me)-OH
CAS Number
114873-06-2
Purity
≥ 99,0 % (HPLC)
Molecular Formula
C15H21Nº4
Molecular Weight
279.34
MDL Number
MFCD01862944
PubChem ID
4393348
Melting Point
68,0-72,0 °C
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = + 13 ± 2 ° (C=1, en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-Fe(3-Me)-OH, Boc- m -Me-L-Phe-OH, Boc-Fe(3-Me)-OH
CAS Number
114873-06-2
Purity
≥ 99,0 % (HPLC)
Molecular Formula
C15H21Nº4
Molecular Weight
279.34
MDL Number
MFCD01862944
PubChem ID
4393348
Melting Point
68,0-72,0 °C
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = + 13 ± 2 ° (C=1, en MeOH)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-3-methyl-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of pharmaceuticals. Its unique structure allows for the incorporation of hydrophobic properties, enhancing the stability of peptide drugs.
  • Drug Development: It is instrumental in the design of new therapeutic agents, especially in the field of cancer research, where modifications to amino acids can lead to more effective treatments. Researchers leverage its properties to create targeted therapies.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to drugs or imaging agents, improving the specificity and efficacy of treatments in targeted drug delivery systems.
  • Protein Engineering: In protein engineering, it aids in the design of proteins with enhanced functionality. The incorporation of this amino acid can lead to proteins with improved binding affinity or stability, which is crucial for various biotechnological applications.
  • Research in Neuroscience: Its derivatives are studied for their potential role in modulating neurotransmitter activity, making it relevant in the development of treatments for neurological disorders, thus contributing to advancements in mental health therapies.

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