58042-45-8 Usage
Description
1-(2,2-diethoxyethoxy)-3-Methylbenzene, also known as diethylene glycol monovinyl ether, is a chemical compound characterized by its molecular formula C11H16O3. It presents as a colorless to pale yellow liquid with a distinct sweet, fruity odor. This versatile compound is recognized for its utility in various industrial applications due to its solvent properties and its role in the production of different types of materials.
Uses
Used in the Solvent Industry:
1-(2,2-diethoxyethoxy)-3-Methylbenzene is used as a solvent for its ability to dissolve a wide range of substances, making it a valuable component in the chemical industry for various processes.
Used in the Production of Resins:
In the resin industry, 1-(2,2-diethoxyethoxy)-3-Methylbenzene is utilized as a key component in the synthesis of resins, contributing to their formation and properties.
Used in Paint and Coating Manufacturing:
1-(2,2-diethoxyethoxy)-3-Methylbenzene is also used as a constituent in the manufacturing of paints and coatings, where its solvent properties aid in the application and drying process of these products.
Used in the Adhesive, Sealant, and Ink Industries:
1-(2,2-diethoxyethoxy)-3-Methylbenzene finds application in the production of adhesives, sealants, and inks, where its chemical composition enhances the performance and workability of these products.
Safety and Handling:
Check Digit Verification of cas no
The CAS Registry Mumber 58042-45-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,4 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58042-45:
(7*5)+(6*8)+(5*0)+(4*4)+(3*2)+(2*4)+(1*5)=118
118 % 10 = 8
So 58042-45-8 is a valid CAS Registry Number.
58042-45-8Relevant articles and documents
Dioxazolones as masked ester surrogates in the Pd(ii)-catalyzed direct C-H arylation of 6,5-fused heterocycles
Saxena, Paridhi,Maida, Neha,Kapur, Manmohan
supporting information, p. 11187 - 11190 (2019/09/30)
A simple and effective Pd(ii)-catalyzed regioselective C(2)-H arylation of 6,5-fused heterocycles with dioxazolones as a masked ester surrogate under mild conditions is reported. The significance of the arylation is highlighted by the new reactivity demonstrated in dioxazolones via proximal C-H activation of the cyclic carbonate of the hydroxamic acid functionality under protic conditions.
Bronchodilator and Antiulcer Phenoxypyrimidinones
Lipinski, C. A.,Stam, J. G.,Pereira, J. N.,Ackerman, N. R.,Hess, H.-J.
, p. 1026 - 1031 (2007/10/02)
Series of 5-phenoxy-2(1H)-pyrimidinones, 5-phenoxy-4(3H)-pyrimidinones, and related compounds were prepared in a follow-up of a lead prepared as a potential cyclic nucleotide regulating agent.Compounds were evaluated for bronchodilator activity in histamine-challenged guinea pigs and for antiulcer activity in a cold-restraint, stressed rat ulcer model.Bronchodilator activity comparable to, or greater than, that of theophylline was found in both the 2(1H)- and 4(3H)-pyrimidinone series and was most prominent in analogues containing either an electron-withdrawing or -donating substituent in the para position of the phenoxy ring.Significant antiulcer activity was observed only in the 2(1H)-pyrimidinone series among three closely related analogues.One of these, 5-(m-methylphenoxy)-2(1H)-pyrimidinone (3), exhibited more potent antiulcer effects than the clinically useful antiulcer agent carbenoxolone, without demonstrating bronchodilator activity.
