87423-83-4

Basic information

• Product Name: 2-(3',5'-Di-tert-butyl-4'-hydroxyphenyl)pyridine
• Synonyms: 2-(3',5'-Di-tert-butyl-4'-hydroxyphenyl)pyridine
• CAS NO: 87423-83-4
• Molecular Weight: 283.414
• Mol File: 87423-83-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(3',5'-Di-tert-butyl-4'-hydroxyphenyl)pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3',5'-Di-tert-butyl-4'-hydroxyphenyl)pyridine(87423-83-4)
• EPA Substance Registry System: 2-(3',5'-Di-tert-butyl-4'-hydroxyphenyl)pyridine(87423-83-4)

Safety Data

• Hazardous Substances Data: 87423-83-4(Hazardous Substances Data)

Upstream product

• 109-04-6 2-bromo-pyridine 
• 27329-74-4 (4-Bromo-2,6-di-tert-butylphenoxy)trimethylsilane 
• 87423-82-3 2,6-di-tert-butyl-4-hydroxy-4-pyridin-2-yl-cyclohexa-2,5-dienone 
• 128-39-2 2,6-di-tert-butylphenol 
• 16110-09-1 2,5 dichloropyridine 
• 859238-53-2 (3,5-di-tert-butyl-4-((trimethyl-silyl)oxy)phenyl)boronic acid 
• 160426-48-2 5-Chloro-2-(3',5'-di-tert-butyl-4'-hydroxyphenyl)pyridine 

Relevant articles and documents

Modulating spin delocalization in phenoxyl radicals conjugated with heterocycles

(Equation Presented) Phenoxyl radicals were synthesized having heterocyclic substituents in the 4-position. Electron spin resonance spectroscopy shows spin density can be modulated by delocalization onto the heterocycle structure, to the extent that some

An efficient synthesis of 4-aryl-2,6-di-tert-butylphenols by a palladium-catalyzed cross-coupling reaction

A series of functionally substituted 4-aryl-2,6-di-tert-butylphenols were prepared by the palladium-catalyzed cross-coupling reaction (Suzuki reaction) of aryl halides with a novel tris[3,5-bis(1,1-dimethylethyl)-4-(trimethylsilyloxy)phenyl]boroxin intermediate.

3,5-Di(t-butyl)-4-hydroxyphenyl substituted pyridines

3,5-Di(t-butyl)-4-hydroxyphenyl and 3,5-di(t-butyl)-4-hydroxybenzoyl-substituted pyridines have pharmacological activity as antiinflammatory agents.