885945-08-4

Upstream product

• 96-97-9 5-nitrosalicylic acid 
• 34841-11-7 methyl 2-methoxy-5-nitrobenzoate 
• 885945-07-3 methyl 3-bromo-2-methoxy-5-nitrobenzoate 

Downstream Products

• 885945-12-0 C₄₆H₇₀N₂O₁₄Si₂ 
• 885945-13-1 C₄₀H₅₄N₂O₁₄ 
• 885945-11-9 C₃₆H₅₂Br₂N₂O₁₄ 
• 885945-10-8 C₁₆H₁₂Br₂N₂O₆ 
• 885945-09-5 C₁₈H₁₆Br₂N₂O₆ 

Relevant academic research and scientific papers

Control over unfolding pathways by localizing photoisomerization events within heterosequence oligoazobenzene foldamers

From the inside out or from the outside in? Two photoswitchable foldamers that incorporate azobenzene moieties as the energy-acceptor units have been designed. The pathway of helix unfolding can be controlled by localizing these photoinduced triggers (sho

Prototype of a photoswitchable foldamer

(Figure Presented) Know where to fold 'em: A foldamer exhibiting a light-induced helix-coil transition (see scheme) can be constructed by introducing a photochromic azobenzene moiety (red) into the center of an amphiphilic phenylene ethynylene backbone (blue). This system gives insight into folding and unfolding mechanisms and promises applications in photoresponsive (bio)materials and "smart" delivery devices based on photoresponsive dynamic receptors.