5182-37-6 Usage
Uses
Used in Chemical Industry:
2,4,4,6-Tetramethyl-1,3-dioxane is used as a solvent for cellulose esters, facilitating the processing and manufacturing of various chemical products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,4,4,6-Tetramethyl-1,3-dioxane is utilized as a solvent in the synthesis of certain drugs, contributing to the development of new medicinal compounds.
Used in Agrochemical Production:
2,4,4,6-Tetramethyl-1,3-dioxane serves as a solvent in the production of agrochemicals, aiding in the formulation of effective agricultural products.
Used as a Stabilizer for Organic Peroxides:
2,4,4,6-Tetramethyl-1,3-dioxane is employed as a stabilizer in the manufacturing process of organic peroxides, enhancing their safety and performance in various applications.
It is crucial to handle 2,4,4,6-Tetramethyl-1,3-dioxane with care due to potential health and safety risks if not used properly, despite its relatively low toxicity.
Check Digit Verification of cas no
The CAS Registry Mumber 5182-37-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5182-37:
(6*5)+(5*1)+(4*8)+(3*2)+(2*3)+(1*7)=86
86 % 10 = 6
So 5182-37-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H11N3OS/c1-8-10(15)12-11(14-13-8)16-7-9-5-3-2-4-6-9/h2-6H,7H2,1H3,(H,12,14,15)
5182-37-6Relevant academic research and scientific papers
AlPO4-Al2O3 PROMOTED CYCLODEHYDRATION OF DIOLS
Costa, A.,Riego, J. M.
, p. 1373 - 1376 (2007/10/02)
A convenient method for the preparation of cyclic ethers by distillation of diols over solid AlPO4-Al2O3 is presented.
COCONDENSATION OF ISOBUTYLENE WITH FORMALDEHYDE AND ACETALDEHYDE
Safarov, M. G.,Ogorodnikov, S. K.,Ibatullin, U.G.,Idlis, G. S.,Nigmatullin, N. G.
, p. 805 - 809 (2007/10/02)
2,4,4-Trimethyl-1,3-dioxane is formed preferentially in the reaction of isobutylene, formaldehyde, and acetaldehyde in the presence of an acidic catalyst.In addition, 4-dimethyl- and 2,4,4,6-tetramethyl-1,3-dioxanes, 4-methyl-2,4-pentanediol and 3-methyl-1,3-butanediol were found in the reaction mass.The possibility of mutual transformations between the cyclic acetals and formal through the stage of the formation of consecutive-parallel reactions is proposed.
