75250-59-8

Usage

Uses

Used in Pharmaceutical Industry:
1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-, methyl ester (9CI) is used as an intermediate compound for the manufacturing of drugs, particularly those related to nicotinic acid and its derivatives. Its role in drug synthesis is attributed to its structural similarity to nicotinic acid, which allows for the development of medications with potential therapeutic benefits.
Used in Food Industry:
In the food industry, 1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-, methyl ester (9CI) serves as a flavoring agent. Its unique properties contribute to the enhancement of flavors in various food products, providing a richer and more diverse taste experience for consumers.
Used in Research and Development:
1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-, methyl ester (9CI) is also utilized in research and development for its potential anti-inflammatory and antioxidant properties. Scientists are studying its therapeutic applications in the treatment of various health conditions, aiming to unlock new possibilities for medical treatments and improve patient outcomes.

Upstream product

• 498-94-2 isonipecotic acid 
• 197585-42-5 1-(methoxycarbonyl)piperidine-4-carboxylic acid 
• 774234-26-3 methyl 4-iodo-1-piperidinecarboxylate 
• 201230-82-2 carbon monoxide 
• 102564-64-7 N-methoxycarbonyl-5-amino-1-penten-3-ol 
• 694-05-3 1,2,3,6-tetrahydropyridine 
• 79-22-1 methyl chloroformate 

Downstream Products

• 56475-87-7 3,4-dihydro-2H-pyridine-1-carboxylic acid methyl ester 
• 75250-52-1 4-hydroxy-piperidine-1-carboxylic acid methyl ester 
• 81396-51-2 methyl (3S*,4R*)-1,2,5,6-tetrahydro-1-piperidinecarboxylate 3,4-oxide 
• 131667-51-1 1-(methoxycarbonyl)-4-phenyl-1,2,3,4-tetrahydropyridine 
• 141090-49-5 1-(methoxycarbonyl)-3-phenyl-1,2,3,4-tetrahydropyridine 
• 75250-40-7 N-carbomethoxy-4-hydroxy-3-(phenylseleno)piperidine 

Relevant academic research and scientific papers

Synthesis of functionalized nitrogen heterocycles by radical decarboxylation of β- and γ-amino acids

Iodinated or oxygenated nitrogen heterocycles are obtained by radical decarboxylation of β- and γ-amino acids. This mild, versatile reaction is applied to the synthesis of bioactive products, such as 4-arylpiperidines, hydroxylated piperidines, and new antifungal agents.

Stereoselective Intramolecular Aminocarbonylation of 3-Hydroxypent-4-enylamides Catalyzed by Palladium

The urethanes and tosamides of 3-Hydroxypent-4-enylamine and its C1-C4 substituted derivatives undergo the palladium catalyzed intramolecular aminocarbonylation (0.1 equiv of PdCl2, 3.0 equiv of CuCl2, 3.0 equiv of NaOAc i

Organic Tellurium and Selenium Chemistry. Reduction of Tellurides, Selenides, and Selenoacetals with Triphenyltin Hydride

Preparative and mechanistic details are described for the conversion of selenides into hydrocarbons RH> by heating with triphenyltin hydride at about 120 deg C.The process has been extended to selenoacetals in a form that constitutes a reduction methods for carbonyl compounds RR'C(SePh)2 -> RR'CH2>.Selective reduction of selenoacetals in the presence of thioacetals is possible.Cold-labeled species can be prepared by using triphenyltin deuteride.Tellurides are available easily without problems arising from exposure to air provided that the work is done in a photographic darkroom equipped with a red safety light.These tellurides, as well as the corresponding dichlorides , are reduced under very mild conditions (25-80 deg C) by triphenyltin hydride.The selenium- and tellurium-based chemistry has been used for the unusual process of reducing an epoxide in the presence of a ketone carbonyl.