218772-96-4

Basic information

• Product Name: (4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE
• Synonyms: (4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE;2-(4-Oxopiperidin-1-yl)acetic acid
• CAS NO: 218772-96-4
• Molecular Formula: C₇H₁₁NO₃
• Molecular Weight: 193.63
• Mol File: 218772-96-4.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: (4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE(218772-96-4)
• EPA Substance Registry System: (4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE(218772-96-4)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 218772-96-4(Hazardous Substances Data)

Usage

General Description

(4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE, also known as oxo-piperidinyl-acetic acid hydrochloride, is a chemical compound with potential pharmaceutical applications. It is a derivative of piperidine and acetic acid, and the hydrochloride salt form makes it more stable and suitable for use in medicinal products. (4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE has been studied for its potential as an analgesic and anti-inflammatory agent, and it may also have applications in the treatment of neurological disorders and psychiatric conditions. Research on (4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE is ongoing, and it shows promise for further development in the pharmaceutical industry.

Upstream product

• 41979-39-9 4-piperidone hydrochloride 
• 79-11-8 chloroacetic acid 
• 5292-43-3 bromoacetic acid tert-butyl ester 
• 40064-34-4 4-piperidone monohydrochloride monohydrate 

Downstream Products

• 56187-37-2 2-(3,5-dichloro-4-oxopyridine-1(4H)-yl)acetic acid 

Relevant articles and documents

Preparation method of 3,5-dihalogenated-4-pyridone-1-acetic acid

The invention provides a preparation method of 3, 5-dihalogenated-4-pyridone-1-acetic acid, and particularly relates to a preparation method of 3,5-dichloro-4-pyridone-1-acetic acid. The method comprises the following steps: performing a substitution reaction on piperidine-4-ketone hydrochloride (II) with chloroacetic acid in the presence of a proper solvent and an acid-binding agent to obtain 4-piperidone-1-acetic acid (III), carrying out a halogenation reaction on the 4-piperidone-1-acetic acid (III) and a halogenation reagent to obtain 3,3,5,5-tetrahalogenated-4-piperidone-1-acetic acid (IV), carrying out an elimination reaction in the presence of an alkali to remove hydrogen halide, and performing acidification with hydrochloric acid to obtain the 3,5-dihalo-4-pyridinone-1-acetic acid.The method has the advantages of cheap and easily available raw materials, low cost, simple operation, easy realization, less wastewater generation amount, environmental protection, high reaction selectivity, high product yield and purity, and suitableness for industrial production.