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1-(4-vinylbenzyl)piperidine, with the molecular formula C15H19N and a molecular weight of 217.31 g/mol, is a piperidine derivative featuring a vinylbenzyl group attached to the piperidine ring. This chemical compound serves as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its unique molecular structure and properties also hold potential for applications in medicinal chemistry and drug development.

4072-75-7

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4072-75-7 Usage

Uses

Used in Organic Synthesis:
1-(4-vinylbenzyl)piperidine is used as a chemical building block for the production of various pharmaceuticals, agrochemicals, and other fine chemicals. Its versatile molecular structure allows for the creation of a wide range of compounds with different applications.
Used in Polymer and Resin Production:
As a monomer, 1-(4-vinylbenzyl)piperidine is utilized in the production of polymers and resins, contributing to the development of materials with specific properties for various industries.
Used in Medicinal Chemistry and Drug Development:
Due to its unique molecular structure and properties, 1-(4-vinylbenzyl)piperidine may have potential applications in medicinal chemistry and drug development, where it could be used as a starting material or a component in the synthesis of novel therapeutic agents.
It is crucial to handle 1-(4-vinylbenzyl)piperidine with care and follow proper safety protocols, as it may present certain hazards associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 4072-75-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4072-75:
(6*4)+(5*0)+(4*7)+(3*2)+(2*7)+(1*5)=77
77 % 10 = 7
So 4072-75-7 is a valid CAS Registry Number.

4072-75-7Downstream Products

4072-75-7Relevant academic research and scientific papers

Aerobic oxidation of amines catalyzed by polymer-incarcerated au nanoclusters: Effect of cluster size and cooperative functional groups in the polymer

Miyamura, Hiroyuki,Morita, Masataka,Inasaki, Takeshi,Kobayashi, Shu

, p. 588 - 599 (2011)

Aerobic oxidation reaction of amines to imines catalyzed by polymer-incarcerated Au nanoclusters (PI-Au) was developed. The effect of cluster size for this oxidation reaction was carefully examined using the same polymer support. We have succeeded in preparation of various PI-Au catalysts containing different size clusters by modification of standard preparation methods. The size of clusters and their distribution were analyzed by electron microscopy. Interestingly, catalysts containing relatively larger clusters (>5 nm) showed higher activity in aerobic oxidation of amines than catalysts containing smaller clusters (13 nm) that showed much better activity for aerobic oxidation of alcohols. In addition, novel Au nanocluster catalysts immobilized on newly prepared polymer with tertiary amine groups were developed and they showed excellent activity for aerobic oxidation of amines to imines. The relation between cluster size and catalytic activity and role of tertiary amine in polymer were discussed. These catalysts could be applied to aerobic oxidative deprotection of p-methoxybenzyl groups.

Functionalized monomers for synthesis of rubbery polymers

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Page 18, (2010/02/05)

This invention discloses a process for synthesizing an amine functionalized monomer that comprises (1) reacting a secondary amine with a 2,3-dihalopropene to produce a vinyl halide containing secondary amine having a structural formula selected from the g

Functionalized monomers for synthesis of rubbery polymers

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Page 15-16, (2010/02/06)

The present invention relates to a rubbery polymer which is comprised of repeat units that are derived from (1) at least one conjugated diolefin monomer, and (2) at least one functionalized monomer of the structural formula: wherein the R′ groups in repea

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