92701-56-9

Usage

Type

Piperidine derivative

Usage

Precursor in the synthesis of pharmaceuticals and other organic compounds

Physical state

Colorless liquid

Odor

Strong

Flammability

Highly flammable

Common use

Reagent in organic chemistry reactions and solvent in certain industrial processes

Toxicity

Moderately toxic

Handling and storage

Handle with care and store in a well-ventilated area

Additional applications

Production of advanced materials, such as polymers and coatings

Upstream product

• 13070-07-0 1-methylpiperidine-2-thione 
• 25355-41-3 1-methyl-6-methylsulfanyl-2,3,4,5-tetrahydro-pyridinium; iodide 
• 622-39-9 2-propylpyridine 
• 3238-60-6 rac-coniine 
• 74-88-4 methyl iodide 
• 92599-71-8 1-(methoxycarbonyl)-2-propylpiperidine 
• 102537-48-4 (S)-6-Propyl-piperidine-1,2-dicarboxylic acid 1-methyl ester 
• 102537-49-5 (S)-2-Methoxy-6-propyl-piperidine-1-carboxylic acid methyl ester 
• 115589-04-3 (2S,6S)-dimethyl 6-propylpiperidine-1,2-dicarboxylate 
• 185385-20-0 6-methoxy-1-methoxycarbonylpipecolate 
• 50-00-0 formaldehyd 
• 562-54-9 potassium methyl sulfate 
• 125133-94-0 N-methylconiine 
• 186045-61-4 (R)-2-Allyl-4-oxo-piperidine-1-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-naphthalen-2-yl-ethyl)-cyclohexyl ester 

Relevant academic research and scientific papers

AMMONIUM SALT, ELECTROLYTE FOR LITHIUM SECONDARY BATTERY, AND LITHIUM SECONDARY BATTERY USING THEM

PROBLEM TO BE SOLVED: To provide: ammonium salt with low viscosity; an electrolyte for a lithium secondary battery; and the lithium secondary battery. SOLUTION: This invention relates to an ammonium salt expressed by the following chemical formula (1). SELECTED DRAWING: None COPYRIGHT: (C)2018,JPO&INPIT

Lewis acid mediated diastereoselective allylation of 3- menthyloxycarbonyl-5,6-dihydropyridin-4-ones

Sakurai allylation of menthyl enoates 5a-c afforded adducts 7a-c with low to excellent facial selectivity, depending on the Lewis acid employed to promote this 1,4-nucleophilic addition of allyltrimethylsilane. A chelated model was assumed to explain the

Lewis acid-promoted asymmetric conjugate allylation of N-acyl-2,3-dihydro-4-pyridones induced by intramolecular π interactions

Lewis acid-promoted conjugate addition reaction of an allylsilane to a series of the chiral 8-arylmenthol-derived N-acyl-2,3-dihydro-4-pyridones leads to the 2-allyl-4-piperidones with moderate to high levels of asymmetric induction, indicating π-stacking contribution to chirality control. This methodology was applied to the asymmetric synthesis of (-)-N-methylconiine. Copyright (C) 1996 Elsevier Science Ltd.

Alkynylation of Thiolactams. New Synthesis of α-Substituted Pyrrolidine and Piperidine Alkaloids

Alkynylation of S-alkylthioamidium salts of thiolactams with lithium acetylides followed by reduction with LiAlH4 provided α-alkynylazacycloalkanes, which on reduction, or hydroboration followed by oxidation, gave α-substituted pyrrolidine and piperidine alkaloids.