89044-58-6 Usage
Uses
Given the provided materials, specific uses for 2,2-dimethyl-5-[(2-methylpiperidin-1-yl)methylidene]-1,3-dioxane-4,6-dione are not explicitly stated. However, based on its structural features, we can hypothesize potential applications:
Used in Pharmaceutical Industry:
2,2-dimethyl-5-[(2-methylpiperidin-1-yl)methylidene]-1,3-dioxane-4,6-dione could be used as a pharmaceutical intermediate for the synthesis of drugs targeting various biological pathways due to the presence of the piperidine ring, which is common in many bioactive molecules.
Used in Chemical Synthesis:
In the chemical synthesis industry, 2,2-dimethyl-5-[(2-methylpiperidin-1-yl)methylidene]-1,3-dioxane-4,6-dione might serve as a building block or reactant in the preparation of more complex organic molecules, leveraging its reactive carbonyl groups and the potential for functional group transformations.
Used in Material Science:
2,2-dimethyl-5-[(2-methylpiperidin-1-yl)methylidene]-1,3-dioxane-4,6-dione could also be explored for its potential use in material science, possibly as a component in the development of new polymers or other materials, given the structural diversity introduced by the dioxane and piperidine rings.
Check Digit Verification of cas no
The CAS Registry Mumber 89044-58-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,4 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89044-58:
(7*8)+(6*9)+(5*0)+(4*4)+(3*4)+(2*5)+(1*8)=156
156 % 10 = 6
So 89044-58-6 is a valid CAS Registry Number.
89044-58-6Relevant academic research and scientific papers
3-Hydroxypyrroles and 1H-Pyrrol-3(2H)-ones. Part 2. Scope and Limitations of the Synthesis of Pyrrol-3-ones by Pyrolysis of Aminomethylene Meldrum's Acid Derivatives.
McNab, Hamish,Monahan, Lilian C.
, p. 863 - 868 (2007/10/02)
Flash vacuum pyrolysis of N,N-disubstituted aminomethylene Meldrum's acid derivatives provides a route to 4,5-unsubstituted 1H-pyrrol-3(2H)-ones by a hydrogen-transfer-cyclisation sequence.Alkyl and aryl 1-substituted, 1,2-disubstituted, and 1,2,2-trisubstituted pyrrolones can be obtained.In competitive cases, there is little selectivity between hydrogen transfer from primary, secondary, or tertiary sites, although benzyl hydrogen atoms proved particularly reactive, giving a general synthesis of 2-phenyl-1H-pyrrol-3(2H)-ones.
