5689-72-5 Usage
Description
1-(Para-methoxyphenyl)-2-methyl-1,3-propanediol methylene ether, a chemical compound with the molecular formula C11H16O3, is a type of propylene glycol ether known for its versatile solvent properties and low volatility. 1-(PARA-METHOXYPHENYL)-2-METHYL-1,3-PROPANEDIOLMETHYLENEETHER is characterized by its ability to dissolve a wide range of substances, making it a preferred choice for various industrial applications.
Uses
Used in the Ink Industry:
1-(Para-methoxyphenyl)-2-methyl-1,3-propanediol methylene ether is used as a solvent for its ability to dissolve various substances, contributing to the production of high-quality inks with consistent performance.
Used in the Paint and Coatings Industry:
As a solvent in the paint and coatings industry, 1-(Para-methoxyphenyl)-2-methyl-1,3-propanediol methylene ether provides a stable and long-lasting solution, ensuring the durability and effectiveness of the final product.
Used in the Production of Polymeric Materials:
1-(Para-methoxyphenyl)-2-methyl-1,3-propanediol methylene ether serves as a coupling agent and a coalescing aid, enhancing the properties of polymeric materials and improving their overall performance.
Used in the Pharmaceutical Industry:
With potential applications in the pharmaceutical industry, 1-(Para-methoxyphenyl)-2-methyl-1,3-propanediol methylene ether can be utilized as an excipient or solvent in drug formulations, thanks to its solvent properties and low volatility.
Check Digit Verification of cas no
The CAS Registry Mumber 5689-72-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5689-72:
(6*5)+(5*6)+(4*8)+(3*9)+(2*7)+(1*2)=135
135 % 10 = 5
So 5689-72-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O3/c1-9-7-14-8-15-12(9)10-3-5-11(13-2)6-4-10/h3-6,9,12H,7-8H2,1-2H3
5689-72-5Relevant articles and documents
The Catalytic Asymmetric Intermolecular Prins Reaction
Diáz-Oviedo, C. David,Maji, Rajat,List, Benjamin
supporting information, p. 20598 - 20604 (2021/12/14)
Despite their significant potential, catalytic asymmetric reactions of olefins with formaldehyde are rare and metal-free approaches have not been previously disclosed. Here we describe an enantioselective intermolecular Prins reaction of styrenes and paraformaldehyde to form 1,3-dioxanes, using confined imino-imidodiphosphate (iIDP) Br?nsted acid catalysts. Isotope labeling experiments and computations suggest a concerted, highly asynchronous addition of an acid-activated formaldehyde oligomer to the olefin. The enantioenriched 1,3-dioxanes can be transformed into the corresponding optically active 1,3-diols, which are valuable synthetic building blocks.
Selective Synthesis of 4-Aryl-1,3-dioxanes from Arylalkenes and Paraformaldehyde using an Ion Exchange Resin as Catalyst; Extension to Natural Compounds
Delmas, Michel,Gaset, Antoine
, p. 871 - 872 (2007/10/02)
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