2418-49-7 Usage
Explanation
The compound is composed of 10 carbon atoms, 14 hydrogen atoms, and 2 oxygen atoms.
Explanation
It belongs to a group of organic compounds that contain a 1,3-dioxane ring structure.
Explanation
This specific isomer has a unique stereochemistry, denoted by the (4R,5R)-reldesignation, which indicates the arrangement of atoms in the molecule.
Explanation
The compound features a 1,3-dioxane ring structure, with a methyl group (CH3) and a phenyl group (C6H5) attached to specific carbon atoms.
Explanation
Due to its unique chemical properties, 1,3-Dioxane, 5-methyl-4-phenyl-, (4R,5R)-rel- is used in the fields of medicine, industry, and research for various purposes.
Explanation
More research is needed to fully understand the properties and potential uses of this chemical compound in different fields.
Explanation
The combination of the 1,3-dioxane ring structure and the methyl and phenyl groups gives 1,3-Dioxane, 5-methyl-4-phenyl-, (4R,5R)-rel- distinct chemical properties that can be exploited in various applications.
Family
Dioxane family
Isomer
(4R,5R)-rel-
Structure
1,3-dioxane ring with methyl and phenyl substituents
Applications
Pharmaceutical and chemical research
Further Research
Ongoing studies and research
Chemical Properties
Unique due to the 1,3-dioxane ring and substituents
Check Digit Verification of cas no
The CAS Registry Mumber 2418-49-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2418-49:
(6*2)+(5*4)+(4*1)+(3*8)+(2*4)+(1*9)=77
77 % 10 = 7
So 2418-49-7 is a valid CAS Registry Number.
2418-49-7Relevant academic research and scientific papers
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.
