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2-hydroxy-1,1,3,3-tetramethyl-2,3-dihydro-1H-isoindole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104653-73-8

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104653-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104653-73-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,5 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104653-73:
(8*1)+(7*0)+(6*4)+(5*6)+(4*5)+(3*3)+(2*7)+(1*3)=108
108 % 10 = 8
So 104653-73-8 is a valid CAS Registry Number.

104653-73-8Downstream Products

104653-73-8Relevant academic research and scientific papers

The Photodynamic Covalent Bond: Sensitized Alkoxyamines as a Tool to Shift Reaction Networks Out-of-Equilibrium Using Light Energy

Herder, Martin,Lehn, Jean-Marie

, p. 7647 - 7657 (2018/06/26)

We implement sensitized alkoxyamines as "photodynamic covalent bonds" - bonds that, while being stable in the dark at ambient temperatures, upon photoexcitation efficiently dissociate and recombine to the bound state in a fast thermal reaction. This type of bond allows for the photochemically induced exchange of molecular building blocks and resulting constitutional variation within dynamic reaction networks. To this end, alkoxyamines are coupled to a xanthone unit as triplet sensitizer enabling their reversible photodissociation into two radical species. By studying the photochemical properties of three generations of sensitized alkoxyamines it became clear that the nature and efficiency of triplet energy transfer from the sensitizer to the alkoxyamine bond as well as the reversibility of photodissociation crucially depends on the structure of the nitroxide terminus. By employing the thus designed photodynamic covalent bonding motif, we demonstrate how to use light energy to shift a dynamic covalent reaction network away from its thermodynamic minimum into a photostationary state. The network could be repeatedly switched between its minimum and kinetically trapped out-of-equilibrium state by thermal scrambling and selective photoactivation of sensitized alkoxyamines, respectively.

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