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2-Methylene-1,3-dioxane, also known as methylenedioxyethane or MDOE, is a colorless, volatile, and highly flammable liquid with the chemical formula C4H6O2. It is an organic compound that consists of a 1,3-dioxane ring with a methylene group (CH2) attached to the 2-position. 2-Methylene-1,3-dioxane is primarily used as a solvent and a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity, 2-methylene-1,3-dioxane can undergo various chemical reactions, such as nucleophilic substitution, electrophilic addition, and rearrangement reactions. It is also known for its potential to form explosive peroxides upon exposure to air, making it necessary to handle it with caution and under controlled conditions.

5663-11-6

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5663-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5663-11-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5663-11:
(6*5)+(5*6)+(4*6)+(3*3)+(2*1)+(1*1)=96
96 % 10 = 6
So 5663-11-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H16N2O/c1-12(19)16-17-14-9-5-6-10-15(14)18(16)11-13-7-3-2-4-8-13/h2-10,12,19H,11H2,1H3

5663-11-6Relevant academic research and scientific papers

Polyesters by a Radical Pathway: Rationalization of the Cyclic Ketene Acetal Efficiency

Gigmes, Didier,Gil, Noémie,Guillaneuf, Yohann,Lefay, Catherine,Plummer, Christopher M.,Siri, Didier,Tardy, Antoine

supporting information, p. 14517 - 14526 (2020/07/13)

Radical ring-opening polymerization (rROP) of cyclic ketene acetals (CKAs) combines the advantages of both ring-opening polymerization and radical polymerization thereby allowing the robust production of polyesters coupled with the mild polymerization conditions of a radical process. rROP was recently rejuvenated by the possibility to copolymerize CKAs with classic vinyl monomers leading to the insertion of cleavable functionality into a vinyl-based copolymer backbone and thus imparting (bio)degradability. Such materials are suitable for a large scope of applications, particularly within the biomedical field. The competition between the ring-opening and ring-retaining propagation routes is a major complication in the development of efficient CKA monomers, ultimately leading to the use of only four monomers that are known to completely ring-open under all experimental conditions. In this article we investigate the radical ring-opening polymerization of model CKA monomers and demonstrate by the combination of DFT calculations and kinetic modeling using PREDICI software that we are now able to predict in silico the ring-opening ability of CKA monomers.

A short and simple synthesis of ketene acetals

Argade,Joglekar

, p. 1979 - 1984 (2007/10/02)

A novel and convenient synthesis of ketene acetals 1a-g in moderate to good yield has been achieved starting from acetonitrile by using Pinner reaction approach.

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