99658-56-7

Usage

Uses

Used in Pharmaceutical Industry:
1-methylpiperidine-3-carbaldehyde is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Its presence in the molecular structure allows for the development of new drugs with potential therapeutic effects.
Used in Agricultural Industry:
1-methylpiperidine-3-carbaldehyde is used as a building block for the production of insecticides and other agrochemicals. Its ability to be incorporated into complex molecules makes it a valuable component in creating effective pest control solutions.
Used in Chemical Industry:
1-methylpiperidine-3-carbaldehyde may also have potential applications in the field of organic chemistry as a reagent in various reactions. Its aldehyde group and piperidine ring provide opportunities for a wide range of chemical transformations and synthesis processes.
Overall, 1-methylpiperidine-3-carbaldehyde has a diverse range of potential uses in the pharmaceutical, agricultural, and chemical industries, making it a versatile compound for research and development.

Upstream product

• 694-55-3 N-methyl-3,4-didehydropiperidine 
• 201230-82-2 carbon monoxide 
• 500-22-1 3-pyridinecarboxaldehyde 
• 99803-15-3 3-(1,3-dioxolan-2-yl)-1-methylpiperidine 
• 105688-89-9 5-(1,3-dioxolan-2-yl)-1-methyl-1,2,3,6-tetrahydropyridine 
• 99803-14-2 3-(1,3-dioxolan-2-yl)-1-methylpyridinium iodide 
• 5740-72-7 3-(ethylenedioxymethyl)pyridine 

Relevant academic research and scientific papers

Pyrrolidinone derivatives, their preparation and pharmaceutical composition comprising the same

The present invention relates to substituted pyrrolidinone compounds of formula 1, wherein n is 0 or 1; Aza is a heterocycle optionally substituted with C1-4 alkyl, or C1-4 alkyl substituted with a heterocycle, which represents a saturated or unsaturated five- or six-membered ring having nitrogen(s) as a heteroatom, which are muscarinic acetylcholine receptor agonists and useful as nootropics and therapeutic agents for cerebral neural diseases such as Alzheimer's disease; and pharmaceutically acceptable salts thereof; processes for the preparation thereof; and pharmaceutical compositions comprising these compounds or salts.

Synthesis of 1'-Methylspiro from 1-Methyl-n-piperidinecarbaldehydes

1'-Methylspiro 2 can be obtained from 1-methyl-n-piperidinecarbaldehydes 1 by the Fischer reaction of their phenylhydrazones.The Fischer reaction provides different kinds of products -3H-indole, indole and oxindole- which depend on the N atom position in the piperidine ring.

Hydroformylation of Nitrogen-Containing Cyclic Olefins via "in-situ" Rhodium-Phosphine Catalysts

Hydroformylation of nitrogen-containing cyclic olefins (N-substituted nortropidines, N-methyl-1,2,3,6-tetrahydropyridine (THP)) with rhodium-PR3 catalysts prepared "in-situ" is reported.The nortropidines reacted rapidly when either trialkyl- or triaryl-type phosphines were used, and the regioselectivities were not significantly influenced by the nature of the phosphine.With the less basic THP the rates and selectivities were generally lower, and were influenced by the phosphine ligand and by the presence of added bases such as Et3N.