262861-04-1 Usage
Description
[2-(4,4-Dimethylpiperidin-1-yl)phenyl]ethanon, also known as DMPP, is a chemical compound that belongs to the class of aromatic ketones. It is characterized by its low volatility and high stability, making it a versatile compound for various industrial applications.
Uses
Used in Stabilizers for Organic Peroxides:
DMPP is used as a stabilizer for organic peroxides, enhancing their performance and ensuring their stability during various industrial processes.
Used in Curing Agents for Resins:
As a curing agent for some resins, DMPP contributes to the hardening and solidification of these materials, which is crucial for their final application and performance.
Used in Pharmaceutical Production:
DMPP is utilized in the production of pharmaceuticals, acting as an intermediate in the synthesis of other organic compounds, which are then used to create various medications.
Used in Synthesis of Other Organic Compounds:
This chemical compound serves as an intermediate in the synthesis of other organic compounds, highlighting its importance in the chemical industry and the development of new materials and products.
Used in Industrial Applications:
Due to its low volatility and high stability, DMPP is suitable for a wide range of industrial applications, where it can be used to improve the properties and performance of various products and materials.
It is important to handle and store DMPP properly, as it can be harmful if ingested, inhaled, or comes into contact with the skin.
Check Digit Verification of cas no
The CAS Registry Mumber 262861-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,2,8,6 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 262861-04:
(8*2)+(7*6)+(6*2)+(5*8)+(4*6)+(3*1)+(2*0)+(1*4)=141
141 % 10 = 1
So 262861-04-1 is a valid CAS Registry Number.
262861-04-1Relevant articles and documents
Participation of electrophilic groups with the dehydrogenation of 4-substituted piperidines
M?hrle,Jeandrée
, p. 74 - 85 (2000)
Dehydrogenation of 2-(1-piperidinyl)-benzaldehydes 1-3 using mercury(II)-EDTA generated the lactams 4-6, indicating a reversible reaction of a carbinolamine intermediate with the formyl group. The yields and oxidation rates decreased by 4-substitution in the piperidine moiety. The 2-(1-piperidinyl)-acetophenones 11, 16-19 showed a similar behavior with mercury(II)-EDTA but gave rise to a product pattern. The trans-benzoquinolizidones 12, 20, 23, 26, 29 resulted from the cyclic iminium compounds reacting with the acetyl group as nucleophile. By another oxidation these species were partially transformed to the quinolinones 13, 21, 24, 27, 30. An intermediate electrophilic neighboring of the carbonyl group with the cyclic hemiaminals led finally to the lactams 14, 22, 25, 28, 31. Mechanisms for the reactions are proposed.
