🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
05229
CAS Number:
137452-49-4
Boc-4-(aminomethyl)-L-phenylalanine
Purity:
≥ 97% (HPLC)
Synonym(s):
Boc-L-Phe(4-CH2NH2)-OH, Boc-p-(aminomethyl)-L-Phe-OH, (S-Boc-2-amino-3-(4-aminomethylphenyl)propionic acid
Documents
$120.88 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-4-(aminomethyl)-L-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for the development of complex peptides and biologically active molecules. Researchers often leverage its unique structure to facilitate the synthesis of peptide-based drugs, particularly in the fields of oncology and immunology, where precise modifications can lead to improved therapeutic efficacy.

The compound's ability to serve as a building block in the synthesis of various peptides allows for the exploration of new drug candidates with enhanced biological activity. Its applications extend to the production of peptide hormones and enzyme inhibitors, showcasing its significance in drug discovery and development. With its favorable properties, Boc-4-(aminomethyl)-L-phenylalanine stands out as a valuable tool for researchers aiming to innovate in the pharmaceutical landscape.

Synonyms
Boc-L-Phe(4-CH2NH2)-OH, Boc-p-(aminomethyl)-L-Phe-OH, (S-Boc-2-amino-3-(4-aminomethylphenyl)propionic acid
CAS Number
137452-49-4
Purity
≥ 97% (HPLC)
Molecular Formula
C15H22N2O4
Molecular Weight
294.32
MDL Number
MFCD01318277
PubChem ID
4067176
Appearance
White to off-white solid
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-Phe(4-CH2NH2)-OH, Boc-p-(aminomethyl)-L-Phe-OH, (S-Boc-2-amino-3-(4-aminomethylphenyl)propionic acid
CAS Number
137452-49-4
Purity
≥ 97% (HPLC)
Molecular Formula
C15H22N2O4
Molecular Weight
294.32
MDL Number
MFCD01318277
PubChem ID
4067176
Appearance
White to off-white solid
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-4-(aminomethyl)-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create specific sequences for studying protein interactions and functions.
  • Drug Development: It plays a significant role in the development of pharmaceuticals, particularly those targeting neurological disorders, due to its ability to modify amino acid structures for enhanced bioactivity.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach drugs or imaging agents to biomolecules, improving the efficacy and targeting of therapeutic agents.
  • Research in Neuroscience: Its structural properties make it valuable in neuroscience research, particularly in studying neurotransmitter systems and developing neuroprotective agents.
  • Custom Synthesis: Many laboratories utilize this compound for custom synthesis projects, providing flexibility in designing experiments tailored to specific research needs.

Citations