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2,2-Dibenzyl-1,3-dioxane is an organic compound with the molecular formula C16H16O2. It is a colorless, crystalline solid that is soluble in organic solvents. This chemical is primarily used as a synthetic intermediate in the production of various pharmaceuticals and agrochemicals. It is synthesized through the reaction of benzyl alcohol with ethylene oxide, followed by cyclization. Due to its potential applications in the synthesis of biologically active compounds, 2,2-dibenzyl-1,3-dioxane has attracted significant interest in the field of organic chemistry.

5695-83-0

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5695-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5695-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,9 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5695-83:
(6*5)+(5*6)+(4*9)+(3*5)+(2*8)+(1*3)=130
130 % 10 = 0
So 5695-83-0 is a valid CAS Registry Number.

5695-83-0Relevant academic research and scientific papers

A Selectivity Study of Activated Ketal Reduction with Borane Dimethyl Sulfide

Bartels, Birgit,Hunter, Roger

, p. 6756 - 6765 (1993)

A chemo- and regioselectivity study of the reagent combination BH3*SMe2/TMSOTf for ketal reduction has been undertaken.It has revealed that simple 1,3-dioxanes reduce cleanly at low temperature in CH2Cl2 while simple 1,3-dioxolanes may give complete ring cleavage and dimerization products.A study of reduction of 4-substituted 1,3-dioxolanes has revealed a solvent-directed regioselectivity which in THF favors the secondary protected derivative.A mechanism is postulated to account for the selectivities based on recent thinking on acetal substitution reactions.

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