31053-73-3 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
1,3-Dioxane,2-(2-naphthalenyl)-(9CI) is a chemical compound derived from dioxane and naphthalene, which are its parent compounds.
Explanation
This compound is commonly used as a solvent in various industrial applications due to its chemical properties.
Explanation
1,3-Dioxane,2-(2-naphthalenyl)-(9CI) is known to have potential toxic effects on humans, including being a possible carcinogen, which means it may cause cancer.
Explanation
The compound is believed to have harmful effects on aquatic organisms and the environment, which necessitates proper handling and disposal to prevent harm.
Explanation
Due to its potential toxic effects and environmental impact, it is crucial to handle and dispose of 1,3-Dioxane,2-(2-naphthalenyl)-(9CI) properly to prevent harm to human health and the environment.
Derivatives
Dioxane and Naphthalene
Industrial Applications
Solvent
Toxic Effects
Potential human carcinogen
Environmental Impact
Harmful to aquatic organisms
Proper Handling and Disposal
Essential for safety
Check Digit Verification of cas no
The CAS Registry Mumber 31053-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,5 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31053-73:
(7*3)+(6*1)+(5*0)+(4*5)+(3*3)+(2*7)+(1*3)=73
73 % 10 = 3
So 31053-73-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H14O2/c1-2-5-12-10-13(7-6-11(12)4-1)14-15-8-3-9-16-14/h1-2,4-7,10,14H,3,8-9H2
31053-73-3Relevant articles and documents
Simple Aza -conjugate addition methodology for the synthesis of isoindole nitrones and 3,4-dihydroisoquinoline nitrones
Peacock, Lucy R.,Chapman, Robert S. L.,Sedgwick, Adam C.,Bull, Steven D.,Mahon, Mary F.,Amans, Dominique
supporting information, p. 994 - 997 (2015/03/18)
Aryl-aldehydes containing ortho-substituted α,β-unsaturated carboxylic acid derivatives react with hydroxylamine to afford reactive N-hydroxy-carbinolamine intermediates that undergo intramolecular aza-conjugate addition reactions to afford isoindole nitrones and 3,4-dihydroisoquinoline nitrones in good yield. Conditions have been developed to reduce these isoindole nitrones to their corresponding hydroxylamine, enamine, and amine derivatives. Isoindole nitrones react with dimethyl acetylenedicarboxylate (DMAD) via a [4 + 2]-cycloaddition/deamination pathway to afford substituted naphthalene derivatives, while 3,4-dihydroisoquinoline nitrones react with DMAD via a [1,3]-dipolar cycloaddition pathway to afford tricyclic heteroarenes.
A METHOD OF ACETALIZING AN ALDEHYDE
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Page/Page column 22; 23; 24, (2013/09/26)
A method of acetalizing an aldehyde comprising reacting said aldehyde with an alcohol in the presence of a polymeric catalyst to form an acetal wherein the polymeric catalyst is a mesoporous poly-melamine-formaldehyde polymer.
