4469-25-4 Usage
Uses
Used in Solvent Applications:
2-Methyl-1,3-dioxepane is used as a solvent in various chemical processes due to its ability to dissolve a wide range of substances. Its low toxicity and mild odor make it a preferred choice for applications where safety and environmental impact are concerns.
Used in Biodegradable Polymer Production:
2-Methyl-1,3-dioxepane serves as a monomer in the production of biodegradable polymers. These polymers are increasingly sought after for their eco-friendly properties, as they can break down naturally in the environment, reducing plastic waste and pollution.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Methyl-1,3-dioxepane is used as a solvent for the synthesis of various drugs and active pharmaceutical ingredients. Its biocompatibility and low toxicity make it an ideal choice for applications involving direct contact with biological systems.
Used in Cosmetics Industry:
2-Methyl-1,3-dioxepane is utilized in the cosmetics industry as a solvent for the formulation of personal care products. Its mild properties and low toxicity ensure the safety of the final products for consumer use.
Used in Biomedical Applications:
Due to its biocompatibility and biodegradability, 2-Methyl-1,3-dioxepane has been studied for potential use in biomedical applications, such as drug delivery systems and medical device coatings. Its properties allow for controlled release of therapeutic agents and reduced environmental impact after use.
Check Digit Verification of cas no
The CAS Registry Mumber 4469-25-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,6 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4469-25:
(6*4)+(5*4)+(4*6)+(3*9)+(2*2)+(1*5)=104
104 % 10 = 4
So 4469-25-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O2/c1-6-7-4-2-3-5-8-6/h6H,2-5H2,1H3
4469-25-4Relevant academic research and scientific papers
Saoud, Mustapha,Romerosa, Antonio,Carpio, Sonia Manas,Gonsalvi, Luca,Peruzzini, Maurizio
, p. 1614 - 1619 (2003)
The water-soluble ruthenium allenylidene complex [{RuCl(μCl)(C=C=CPh2)(TPPMS)2}2] Na4 catalyses the selective transformation of substituted linear and cyclic vinyl ethers with MeOH, under mild non acidic conditions, to give acetals, while aldehydes and ketones are obtained in a CHCl3/H2O mixture, which allows for easy recycling of the catalyst. NMR studies showed that the reaction follows a transetherification mechanism rather than simple acid-catalysed hydrolysis. ( Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).
PYROLYTIC TRANSFORMATION OF THE VINYL MONOETHERS OF DIOLS IN THE PRESENCE OF ALKALIS
Trofimov, B. A.,Oparina, L. A.,Parshina, L. N.,Lavrov, V. I.,Grigorenko, V. I.,Zhumabekov, M. K.
, p. 1424 - 1428 (2007/10/02)
The alkaline pyrolysis of the vinyl monoethers of diols takes place at 170-250 deg C and is accompanied by cycloacetalization (ethylene glycol, 1,3-propanediol), by processes involving cleavage of the C-O bonds (diethylene glycol, 1,4-butanediol), and also by the release of hydrogen, carbon dioxide, methane, ethane, acetylene, and C3 to C5 hydrocarbons.Distillation of ethylene glycol vinyl monoether with potassium hydroxide, sodium hydroxide, and lithium hydroxide can result in explosion as a result of the vigorous and exothermic release of gas.
