1401429-23-9

Basic information

• Product Name: C₂₀H₁₉N₅O₈S₂*C₃₆H₆₀O₃₀
• CAS NO: 1401429-23-9
• Molecular Weight: 1494.39
• Mol File: 1401429-23-9.mol

Chemical Properties

• CAS DataBase Reference: C₂₀H₁₉N₅O₈S₂*C₃₆H₆₀O₃₀(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₀H₁₉N₅O₈S₂*C₃₆H₆₀O₃₀(1401429-23-9)
• EPA Substance Registry System: C₂₀H₁₉N₅O₈S₂*C₃₆H₆₀O₃₀(1401429-23-9)

Safety Data

• Hazardous Substances Data: 1401429-23-9(Hazardous Substances Data)

Upstream product

• 1401429-20-6 7-((4-(2-(2-azidoethoxy) ethoxy) phenyl) diazenyl)naphthalene-1,3-disulfonic acid 
• 10016-20-3 alpha cyclodextrin 

Downstream Products

• 1401429-22-8 C₃₁H₂₇N₅O₁₃S₂*C₃₆H₆₀O₃₀ 

Relevant articles and documents

NIR-triggered drug release from switchable rotaxane-functionalized silica-covered Au nanorods

An NIR-triggered drug delivery system was developed by capping photo-switchable azobenzene-based rotaxane onto Au nanorod-mesoporous silica core-shell hybrids. Drug release from the nanocarrier in zebrafish embryo models could be controlled remotely under

Photothermal-responsive [2]rotaxanes

Three photothermal-responsive α-cyclodextrin-based [2]rotaxanes were prepared via the copper(i)-catalyzed azide-alkyne cycloaddition, in which the α-cyclodextrin ring was threaded onto the azobenzene dumbbell component. The difference between the three [2]rotaxanes are the length of the ethylene glycol repeating chains connected between the azobenzene and triazole units in the dumbbell components. The α-cyclodextrin rings in the [2]rotaxanes can be reversibly switched between the azobenzene unit and triazole/ethylene glycol unit driven by the trans-cis isomerization of the azobenzene unit. The trans-to-cis isomerization of the azobenzene unit under UV light irradiation (365 nm) leads the α-cyclodextrin ring moving to the triazole/ethylene glycol unit, while the cis-to-trans isomerization of the azobenzene unit under either visible light irradiation or heating enables the α-cyclodextrin ring shuttling back to the azobenzene station. The different ethylene glycol repeating chains in the [2]rotaxanes can affect (1) the isomerization rates of the azobenzene units, i.e. the longer the chain, the faster the isomerization rate, and (2) fluorescent quantum yields of the [2]rotaxanes, i.e. the longer the chain, the lower the fluorescent quantum yield. In addition, the quantum yields of the [2]rotaxanes were enhanced by UV light irradiation and decreased back upon visible light irradiation or heating at 65 °C. The current research provides a fundamental understanding of the working mechanism for photothermal-responsive [2]rotaxanes.