75250-59-8

Basic information

• Product Name: 1(2H)-Pyridinecarboxylicacid,3,6-dihydro-,methylester(9CI)
• Synonyms: 1(2H)-Pyridinecarboxylicacid,3,6-dihydro-,methylester(9CI)
• CAS NO: 75250-59-8
• Molecular Formula: C₇H₁₁NO₂
• Molecular Weight: 0
• Product Categories: CARBOXYLICESTER
• Mol File: 75250-59-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1(2H)-Pyridinecarboxylicacid,3,6-dihydro-,methylester(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1(2H)-Pyridinecarboxylicacid,3,6-dihydro-,methylester(9CI)(75250-59-8)
• EPA Substance Registry System: 1(2H)-Pyridinecarboxylicacid,3,6-dihydro-,methylester(9CI)(75250-59-8)

Safety Data

• Hazardous Substances Data: 75250-59-8(Hazardous Substances Data)

Usage

General Description

1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-, methylester (9CI) is a chemical compound that is also known as nicotinic acid methyl ester. It is a derivative of nicotinic acid and is commonly used in the manufacturing of drugs, particularly those related to nicotinic acid and its derivatives. It is also used as a flavoring agent in the food industry. 1(2H)-Pyridinecarboxylicacid,3,6-dihydro-,methylester(9CI) is known for its potential anti-inflammatory and antioxidant properties, and it is being studied for its potential therapeutic applications in the treatment of a variety of health conditions. However, it should be handled and used with caution due to its potential toxicity.

Upstream product

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

Downstream Products

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

Relevant articles and documents

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