1420844-67-2

Upstream product

• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 
• 13122-89-9 (S)-methyl 2-((S)-2-(tert-butoxycarbonylamino)-3-phenylpropanamido)-3-phenylpropanoate 
• 13122-90-2 Boc-Phe-Phe-OH 
• 28097-02-1 methyl 4-[(E)-2-(4-aminophenyl)ethenyl]benzoate 
• 1420844-61-6 C₃₉H₄₁N₃O₆ 
• 24424-99-5 di-tert-butyl dicarbonate 
• 540-37-4 p-aminoiodobenzene 
• 159217-89-7 N-Boc-4-iodoaniline 
• 1075-49-6 4-ethenylbenzoic acid 
• 1076-96-6 methyl 4-vinylbenzoate 
• 1565-41-9 p-vinylbenzoyl chloride 
• 63-91-2 L-phenylalanine 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 

Relevant academic research and scientific papers

A synthetic amino acid residue containing a new oligopeptide-based photosensitive fluorescent organogel

A synthetic amino acid (with a stilbene residue in the main chain) containing a tripeptide-based organogelator has been discovered. This peptide-based synthetic molecule 1 self-assembles in various organic solvents to form an organogel. The gel has been thoroughly characterized by using various microscopic techniques including field-emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), X-ray diffraction (XRD), UV-visible and fluorescence spectroscopy, and rheology. Morphological investigations using FESEM and AFM show a nanofibrillar network structure. Interestingly, the organogel is photoresponsive and a gel-sol transition occurred by irradiating the gel with UV light of 365 nm for 2 h as shown by the UV and fluorescence study. This photoresponsive fluorescent gel holds promise for new peptide-based soft materials with interesting applications. Copyright