1393604-89-1

Basic information

• Product Name: C₂₃H₂₉NO₉S
• CAS NO: 1393604-89-1
• Molecular Weight: 495.551
• Mol File: 1393604-89-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₂₃H₂₉NO₉S(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₃H₂₉NO₉S(1393604-89-1)
• EPA Substance Registry System: C₂₃H₂₉NO₉S(1393604-89-1)

Safety Data

• Hazardous Substances Data: 1393604-89-1(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 112-60-7 Tetraethylene glycol 
• 37860-51-8 tetraethylene glycol di(p-toluenesulfonate) 
• 6253-28-7 3,6-epoxy-1,2,3,6-tetrahydrophthalimide 

Downstream Products

• 1393604-90-4 C₁₈H₂₅NO₇S 

Relevant articles and documents

Dendritic architectures by orthogonal thiol-maleimide "click" and furan-maleimide dynamic covalent chemistries

A set of dendrons and dendrimers is synthesized divergently using an orthogonal combination of kinetically-driven thiol-maleimide "click" chemistry and thermodynamically reversible furan-maleimide cycloaddition/retrocycloaddition reactions. Growth is controlled by taking advantage of the selective thiol-ene addition of thiols to the electron withdrawn alkene of maleimide in the presence of electron rich alkene of oxanorbornene. Subsequent activation of growing dendrons/dendrimers requires only heat to induce the dynamic covalent liberation of peripheral furan protecting groups. The methodology introduced provides a new route to multifunctional dendrimers that could, in principle, be synthesized by introducing different branched monomers at any stage of dendrimer growth, allowing dendrimer architectures and properties to be better tailored to their intended applications.