182310-66-3

Upstream product

• 149826-78-8 4-t-butyl-2-(5-t-butyl-3-chloromethylsalicyloyl)-6-chloromethylphenol 
• 25446-98-4 2,2'-dihydroxy-5,5'-di-tert-butylbenzophenone 
• 98-54-4 para-tert-butylphenol 
• 50-00-0 formaldehyd 
• 149790-91-0 4-t-butyl-2-<5-t-butyl-3-<5-t-butyl-3-(5-t-butylsalicyl)salicyloyl>salicyl>phenol 

Downstream Products

• 182310-73-2 {5-tert-Butyl-3-[5-tert-butyl-3-(5-tert-butyl-2-hydroxy-benzyl)-2-hydroxy-benzyl]-2-hydroxy-phenyl}-{5-tert-butyl-3-[5-tert-butyl-3-(5-tert-butyl-2-hydroxy-3-hydroxymethyl-benzyl)-2-hydroxy-benzyl]-2-hydroxy-phenyl}-methanone 
• 182310-69-6 Bis-{5-tert-butyl-3-[5-tert-butyl-3-(5-tert-butyl-2-hydroxy-benzyl)-2-hydroxy-benzyl]-2-hydroxy-phenyl}-methanone 

Relevant academic research and scientific papers

Syntheses of p-tert-butyloxocalix[4]-, [5]-, and [6]arenes and their behavior in solution

p-tert-Butyloxocalix[4]-, [5]-, [6]arenes were synthesized by a stepwise procedure. NMR studies demonstrated that strong intramolecular hydrogen bonding between the bridging CO and neighboring phenolic OH groups in the oxocalixarenes weakened the circular