82962-58-1

Basic information

• Product Name: Ibuprofen piconol
• Synonyms: Benzeneacetic acid, α-methyl-4-(2-methylpropyl)-, 2-pyridinylmethyl ester, (-)-;Benzeneacetic acid,a-Methyl-4-(2-Methylpropyl)-,2-pyridinylMethyl ester
• CAS NO: 82962-58-1
• Molecular Formula: C19H23NO2
• Molecular Weight: 297.39
• Mol File: 82962-58-1.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ibuprofen piconol(CAS DataBase Reference)
• NIST Chemistry Reference: Ibuprofen piconol(82962-58-1)
• EPA Substance Registry System: Ibuprofen piconol(82962-58-1)

Safety Data

• Hazardous Substances Data: 82962-58-1(Hazardous Substances Data)

Upstream product

• 586-98-1 2-Hydroxymethylpyridine 
• 15687-27-1 ibuprofen 
• 61566-34-5 (+/-)-ibuprofen methyl ester 
• 71381-91-4 (+/-)-2-(4-isobutylphenyl)propanoyl chloride 
• 2387-23-7 1,3-Dicyclohexylurea 

Relevant articles and documents

METHOD FOR PRODUCING ESTER GROUP-CONTAINING COMPOUND

The present invention provides a novel method for producing an ester group-containing compound and a derivative produced using the compound as a synthetic intermediate. The invention also provides a polymerizable composition containing the compound obtained by the production method and a film-shaped polymer obtained by polymerizing the polymerizable composition. The present invention is a method for producing an ester group-containing compound, the method including a mixing step of mixing a condensing agent, a Bronsted acid, a carboxylic acid, and a phenol or an alcohol to prepare a reaction mixture. The Bronsted acid selected is other than the condensing agent, the carboxylic acid, and the phenol.

ZINC COMPLEX

A zinc complex characterized in exhibiting an octahedral structure and being configured from repeating units represented by general formula (I): wherein L represents a linker region, and R1 represents a C1-4 alkyl group, which can have a halogen atom.

A green chemistry approach to ibuprofen piconol

Ibuprofen piconol synthesis has been described. The use of solid catalyst has demonstrated green chemistry approach with promoted atom economy of 94% compared to the reported 68%.