7062-57-9

Usage

Molecular structure

1-(4-tert-butylphenyl)-2-(5-methylpyridin-2-yl)-1,2-dihydrochromeno[2,3-c]pyrrole-3,9-dione has a complex molecular structure with a chromeno[2,3-c]pyrrole core and substituents of 4-tert-butylphenyl and 5-methylpyridin-2-yl groups.

Chemical class

It belongs to the class of dihydrochromeno[2,3-c]pyrrole-3,9-diones.

Biological activities

Due to its chemical complexity, it is likely to have diverse biological activities.

Pharmacological applications

It has potential pharmacological applications, but further research is needed to determine its specific properties and potential uses.

Industrial applications

Its potential uses in various scientific and industrial fields are still under investigation.

Research necessity

Further research is required to fully understand its properties and potential applications.

Upstream product

• 1611-07-0 3,5-Di-tert-butyl-4-hydroxyphenylacetonitrile 
• 2091-51-2 4-(bromomethyl)-2,6-di-tert-butylphenol 
• 1620-98-0 3,5-di-t-butyl-4-hydroxybenzaldehyde 
• 7019-95-6 4-(piperidino)methylene-2,6-di-tert-butylcyclohexa-2,5-dien-1-one 
• 23093-92-7 cyano(piperidino)(3,5-ditert-butyl-4-hydroxyphenyl)methane 
• 75-05-8 acetonitrile 

Downstream Products

• 77380-02-0 2,6-ditert-butyl-7-cyano-7-piperidinoquinone methide 
• 77380-03-1 Dicyano(piperidino)(3,5-ditert-butyl-4-hydroxyphenyl)methane 
• 67341-88-2 4-bis(piperidino)methylene-2,6-di-tert-butyl-2,5-cyclohexadienone 
• 23093-92-7 cyano(piperidino)(3,5-ditert-butyl-4-hydroxyphenyl)methane 

Relevant academic research and scientific papers

Easy large scale syntheses of 2,6-di-t-butyl7-cyano-, 7-carboxy- and 7- methoxycarbonyl quinone methides

Easy large scale syntheses of 2,6-di-t-butyl-7-cyano-, 7-carboxy- and 7- methoxycarbonyl quinone methides 1-3 using cheap and readily available starting materials have been developed.

7-substituted quinone methides as inhibitors for unsaturated monomers

Ethylenically unsaturated monomers are protected from premature polymerization during manufacture and storage by the incorporation therein of an effective stabilizing amount of a 7-substituted quinone methide compound.

Electrochemical Oxidation, VII. Synthesis and Structure of 7-tert-Butyl-2-methylbenzoxazoles

Anodic oxidation of 15 tert-butylphenols 1a - o in absolute acetonitrile or acetonitrile/perchloric acid leads to the corresponding 7-tert-butyl-2-methylbenzoxazoles 3a - o.The proof of the structure was achieved by independent synthesis of 3k, and by 13C NMR spectroscopy as well as by X-ray analysis of 7-tert-butyl-2-methyl-5-benzoxazolecarbaldehyde (3j).The influence of the supporting electrolyte on the formation of the oxidation products is discussed.