4362-22-5 Usage
Description
1,3-DIOXOLANE, 2-(1-PHENYLETHYL) is a dioxolane derivative featuring a 1,3-dioxolane ring with a 1-phenylethyl group attached at the 2nd position. This organic compound is characterized by its unique structure and potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
1,3-DIOXOLANE, 2-(1-PHENYLETHYL) is used as an intermediate compound for the synthesis of various pharmaceutical products. Its unique structure allows it to be a key component in the development of new drugs, potentially contributing to the treatment of various medical conditions.
Used in Chemical Synthesis:
In the field of organic chemistry, 1,3-DIOXOLANE, 2-(1-PHENYLETHYL) serves as a valuable building block for the creation of more complex molecules. Its versatile structure makes it suitable for use in the synthesis of a wide range of chemical products, including specialty chemicals and advanced materials.
Used in Research and Development:
Due to its unique properties, 1,3-DIOXOLANE, 2-(1-PHENYLETHYL) is utilized in research and development settings to explore new chemical reactions and investigate its potential applications in various fields. This may lead to the discovery of novel uses and advancements in related industries.
Used in Flavor and Fragrance Industry:
The specific chemical structure of 1,3-DIOXOLANE, 2-(1-PHENYLETHYL) may also find applications in the flavor and fragrance industry, where it could be used to create unique scents and flavors for various products.
Check Digit Verification of cas no
The CAS Registry Mumber 4362-22-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4362-22:
(6*4)+(5*3)+(4*6)+(3*2)+(2*2)+(1*2)=75
75 % 10 = 5
So 4362-22-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O2/c1-9(11-12-7-8-13-11)10-5-3-2-4-6-10/h2-6,9,11H,7-8H2,1H3
4362-22-5Relevant articles and documents
Visible-light-induced acetalization of aldehydes with alcohols
Yi, Hong,Niu, Linbin,Wang, Shengchun,Liu, Tianyi,Singh, Atul K.,Lei, Aiwen
supporting information, p. 122 - 125 (2017/11/27)
In this work, we have achieved a simple and general method for acetalization of aldehydes by means of a photochemical reaction under low-energy visible light irradiation. A broad range of aromatic, heteroaromatic, and aliphatic aldehydes have been protected under neutral conditions in good to excellent yields using a catalytic amount of Eosin Y as the photocatalyst. Our visible light mediated acetalization strategies are successful for more challenging acid-sensitive aldehydes and sterically hindered aldehydes. Notably, this protocol is chemoselective to aldehydes, while ketones remain intact.
Formation of acetals under rhodium-catalyzed hydroformylation conditions in alcohols
Diebolt, Olivier,Cruzeuil, Clement,Mueller, Christian,Vogt, Dieter
supporting information; experimental part, p. 670 - 677 (2012/04/23)
Hydroformylation of terminal alkenes in alcohol solvents leads to the selective formation of the corresponding acetals. The Xantphos ligand gave the best results as well as acetal selectivities higher than 99% and linear/branched ratios of up to 52 were obtained. The scope of the reaction was studied. Acetals were found to be unreactive under hydroaminomethylation conditions. Copyright
Acetalization of carbonyl compounds catalyzed by bismuth triflate under solvent-free conditions
Aliyan, Hamid,Fazaeli, Razieh,Massah, Ahmad Reza,Momeni, Ahmad Reza,Naghash, Hamid Javaherian,Moeinifard, Behzad
experimental part, p. 873 - 876 (2012/04/05)
Carbonyl compounds were converted to the corresponding 1,3-dioxolanes and 1,3-dioxanes with ethylene glycol and 1,3-propandiol in the presence of bismuth triflate under solvent-free conditions. In addition, high chemoselective protection of aldehydes in the presence of ketones has been achieved.
