32102-41-3

Upstream product

• 739-92-4 1,4-diacetoxy-2,6-di-t-butylbenzene 
• 489-01-0 2,6-Di-t-butyl-4-methoxyphenol 
• 75169-17-4 4-acetoxy-3,5-di-tert-butylanisole 

Downstream Products

• 157360-54-8 4-acetoxy-3,5-di-tert-butyl-1-(2-methyl-2-propenyloxy)benzene 
• 157360-29-7 5-acetoxy-4,6-di-tert-butyl-2-hydroxybenzaldehyde 
• 1026316-66-4 acetic acid 2,6-di-tert-butyl-4-hydroxy-3-(1-hydroxy-2-octyl-decyl)-phenyl ester 
• 1025928-19-1 acetic acid 2,6-di-tert-butyl-3-(2-heptyl-1-hydroxy-nonyl)-4-hydroxy-phenyl ester 
• 173662-47-0 4-acetoxy-3,5-di-tert-butyl-2-(1-hydroxy-2-pentylheptyl)phenol 
• 157360-66-2 4-acetoxy-3,5-di-tert-butyl-2-[1-hydroxy-5-methyl-2-(3-methylbutyl)hexyl]phenol 
• 1027047-00-2 acetic acid 2,2-dibenzyl-4,6-di-tert-butyl-2,3-dihydro-benzofuran-5-yl ester 
• 1026078-80-7 acetic acid 2,6-di-tert-butyl-3-(cycloheptyl-hydroxy-methyl)-4-hydroxy-phenyl ester 
• 1026940-82-8 acetic acid 2,6-di-tert-butyl-4-hydroxy-3-[hydroxy-(tetrahydro-pyran-4-yl)-methyl]-phenyl ester 
• 157360-61-7 4-acetoxy-3,5-di-tert-butyl-2-(2-ethyl-1-butenyl)phenol 
• 173662-54-9 4-acetoxy-3,5-di-t-butyl-2-(2-methyl-2-propenyl)phenol 
• 157360-67-3 4-acetoxy-3,5-di-tert-butyl-2-(2-propenyl)anisole 
• 157360-56-0 4-acetoxy-3,5-di-tert-butyl-2-(2-propenyl)phenol 
• 157360-68-4 4-acetoxy-3,5-di-tert-butyl-2-formylmethylanisole 

Relevant academic research and scientific papers

Novel phenolic antioxidant-functionalized dendritic polyethylene: Synthesis by tailor-made nickel(II) α-diimine-catalyzed copolymerization and its characteristics as non-releasing additive

This work describes a simple one-pot and controlled synthetic method to generate migration-resistant bio-friendly tailor-made antioxidants through ethylene–sterically hindered phenolic antioxidant (SHPA) copolymerization by coordination polymerization usi

Process for preparation of a benzofuran derivative

An industrially useful process for producing benzofuran derivatives of formula (1) by formylating a compound of formula (2) (where A1 is a protective group), followed by reaction with a compound of formula (4) (where X1 is a halogen atom), then performing a cyclizing reaction and subsequently performing a reaction for hydroxyl group deprotection.

Design and synthesis of 4,6-di-tert-butyl-2,3-dihydro-5-benzofuranols as a novel series of antiatherogenic antioxidants

Antioxidants have been considered as potential antiatherogenic agents by inhibiting oxidation of low-density lipoprotein (LDL), albeit vitamin E, a natural antioxidant, has failed to show reduction on atherosclerosis in clinical trials. We have rationally

4,6 Di-t-butyl-5-hydroxy-2,3-dihydrobenzothiophene

A compound represented by formula (I): STR1 wherein R1 represents a hydrogen atom, a lower alkyl group or an acyl group; R2 and R3, which may be the same or different, each represents a hydrogen atom, an optionally substit

4,6-Di-t-butyl-dihydrobenzofuran-5-ol and its derivatives

Compounds represented by the general formula as well as intermediates for the synthesis of thereof: STR1 where R1 is a hydrogen atom or an acyl group; R2 is a lower alkyl group; R3 is a hydrogen atom or a lower alkyl group