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66822-20-6

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66822-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66822-20-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,2 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66822-20:
(7*6)+(6*6)+(5*8)+(4*2)+(3*2)+(2*2)+(1*0)=136
136 % 10 = 6
So 66822-20-6 is a valid CAS Registry Number.

66822-20-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name α,α'-dimethoxybenzyl radical

1.2 Other means of identification

Product number -
Other names 2,2-dimethoxybenzyl radical

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:66822-20-6 SDS

66822-20-6Relevant academic research and scientific papers

NIR Light-Induced ATRP for Synthesis of Block Copolymers Comprising UV-Absorbing Moieties

Kütahya, Ceren,Meckbach, Nicolai,Strehmel, Veronika,Gutmann, Jochen S.,Strehmel, Bernd

, p. 10444 - 10451 (2020/07/27)

NIR exposure at 790 nm activated photopolymerization of monomers comprising UV-absorbing moieties by using [CuII/(TPMA)]Br2 (TPMA=tris(2-pyridylmethyl)amine) in the ppm range and an alkyl bromide as initiator. Some of them comprised structural elements selected either from those showing proton transfer or photocycloaddition upon UV excitation. Polymers obtained comprise living end groups serving as macroinitiator for controlled synthesis of block copolymers with relatively narrow molecular weight distributions. Chromatographic results indicated formation of block copolymers produced by this synthetic approach. Free-radical polymerization of monomers pursued for comparison exhibited the expected broader dispersity of molecular weight compared to photo-ATRP. Polymerization of these monomers by UV photo-ATRP failed on the contrary to NIR photo-ATRP demonstrating the UV-filter function of the monomers. This work conclusively provides a new approach for the polymerization of monomers comprising UV-absorbing moieties through photo-ATRP in the NIR region. This occurred in a simple and efficient pathway. However, studies also showed that not all monomers chosen successfully proceeded in the NIR photo-ATRP protocol.

Synthesis and characterization of cyclohexene oxide functional polystyrene macromonomers by ATRP and their use in photoinitiated cationic polymerization

Degirmenci, Mustafa,Izgin, Oner,Acikses, Aslisah,Genli, Nasrettin

scheme or table, p. 28 - 34 (2011/12/16)

In this study, a novel well-defined macromonomer of epoxy end-functionalized polystyrene was synthesized by atom transfer radical polymerization (ATRP). The compound 3-cyclohexenylmethyl-2-bromopropanoate was synthesized by the condensation of 3-cyclohexe

Effect of nitroxide radicals on chemically induced dynamic electron polarization of spin-correlated radical pairs in aqueous micellar solutions of sodium dodecyl sulfate

Gorelik,Tarasov,Shakirov,Bagryanskaya

experimental part, p. 1416 - 1427 (2009/09/30)

The multispin systems consisting of spin-correlated radical pairs (SCRPs) and stable nitroxide radicals, localized in micelles of sodium dodecyl sulfate (SDS), were studied by ESR and pulse laser photolysis techniques. In all the systems studied, the stab

EPR and computational studies of the formation and β-scission of cyclic and acyclic dialkoxyalkyl radicals

Feilding,Franchi,Roberts,Smits

, p. 155 - 163 (2007/10/03)

EPR spectroscopy and density functional theory have been applied to study the formation and subsequent β-scission of a series of dialkoxyalkyl radicals. Abstraction of hydrogen by photochemically-generated tert-butoxyl radicals from acyclic acetals R1O(R2O)CHR3, and from cyclic analogues derived from diols, takes place mainly from the acetal carbon atom to give radicals of the type R1O(R2O)CR3 and relative rates of abstraction have been determined in competition experiments. When R3 = phenyl or vinyl, the activating influence of these substituents on hydrogen-atom abstraction is smaller than might be expected, probably because delocalisation of the unpaired electron on to the unsaturated group comes at the expense of planarisation at Cα, in opposition to the natural pyramidalising tendency of the two α-alkoxy groups. Absolute rate constants and Arrhenius activation parameters for β-scission of R1O(R2O)CR3 have been determined by a steady-state EPR method and the results can be understood in terms of angle-strain and stereoelectronic effects. β-Scission of selected cyclic dialkoxyalkyl radicals that carry a phenyl or vinyl substituent at the radical centre has been investigated using density functional theory at the UB3LYP/6-31G(d,p) level. Computed activation parameters are in good agreement with the experimental results, where comparison is possible. Both experiment and theory indicate that benzylic 2-phenyl-1,3-dioxan-2-yl radicals undergo β-scission more readily than the corresponding allylic 2-vinyl-1,3-dioxan-2-yl radicals.

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