133747-58-7

Basic information

• Product Name: methyl 5-oxo-1-(p-tolyl)pyrrolidine-3-carboxylate
• Synonyms: methyl 5-oxo-1-(p-tolyl)pyrrolidine-3-carboxylate
• CAS NO: 133747-58-7
• Molecular Weight: 233.267
• Mol File: 133747-58-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 5-oxo-1-(p-tolyl)pyrrolidine-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 5-oxo-1-(p-tolyl)pyrrolidine-3-carboxylate(133747-58-7)
• EPA Substance Registry System: methyl 5-oxo-1-(p-tolyl)pyrrolidine-3-carboxylate(133747-58-7)

Safety Data

• Hazardous Substances Data: 133747-58-7(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 133747-57-6 1-(4-methylphenyl)-5-oxopyrrolidine-3-carboxylic acid 
• 97-65-4 2-methylenesuccinic acid 
• 106-49-0 p-toluidine 
• 617-52-7 Dimethyl itakonate 

Downstream Products

• 331727-49-2 5-oxo-1-(p-tolyl)pyrrolidine-3-carbohydrazide 
• 1342800-22-9 1-(4-methylphenyl)-5-oxo-N'-(4-oxo-1,4-dihydronaphthalen-1-ylidene)pyrrolidine-3-carbohydrazide 
• 1342800-40-1 N'-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-1-(4-methylphenyl)-5-oxopyrrolidine-3-carbohydrazide 
• 1342800-36-5 N-ethyl-N'-(3-methyl-4-oxo-1,4-dihydronaphthalen-1-yl)-1-(4-methylphenyl)-5-oxopyrolidine-3-carbohydrazide 
• 1342800-29-6 N'-(3-methyl-4-oxo-1,4-dihydronaphthalen-1-ylidene)-1-(4-methylphenyl)-5-oxopyrrolidine-3-carbohydrazide 
• 133747-60-1 Methyl 4-[1-(4-tolyl)-2-pyrrolidon-4-yl]methoxybenzoate 
• 133747-61-2 Methanesulfonic acid 5-oxo-1-p-tolyl-pyrrolidin-3-ylmethyl ester 
• 133747-59-8 1-(4-Tolyl)-4-hydroxymethyl-2-pyrrolidone 

Relevant articles and documents

Efficient novel eutectic-mixture-mediated synthesis of benzoxazole-linked pyrrolidin-2-one heterocycles

In this study, new benzoxazole-linked pyrrolidinone heterocyclic compounds were synthesized by an eco-efficient strategy using substituted benzylamines and 2-aminophenol under ultrasonic irradiation in the presence of a newly designed metal-free deep eutectic solvent (DES). This DES was prepared by using a eutectic mixture of urea and a synthesized glycine-derived ionic liquid. X-ray diffraction and infrared spectroscopy were employed to investigate the structure of the ionic liquid and characterize the DES, respectively. This method exhibited key advantages of high productivity, a short reaction time, and simple processing. Moreover, this DES was easily separated from reaction mixtures and can be recycled for multiple reactions.

Synthesis of 4-methyloxybenzoic acids and related compounds, and their inhibitory capacities toward fatty-acid and sterol biosynthesis

The synthesis of a series of 4-methyloxybenzoic acids and related compounds, and their evaluation for inhibitory capacity toward fatty-acid and sterol biosyntheses using rats' liver slices in vitro and rabbits