992-52-9

Upstream product

• 98-54-4 para-tert-butylphenol 
• 2467-07-4 bis(5-tert-butyl-2-hydroxy-3-hydroxymethyl-phenyl)methane 
• 182946-02-7 2-(3-chloromethyl-2-hydroxy-5-tert-butylbenzyl)-6-chloromethyl-4-tert-butylphenol 
• 50-00-0 formaldehyd 
• 112387-50-5 C₃₃H₄₄O₄ 
• 908-17-8 3-Chlor-2,2'-dihydroxy-3'-hydroxymethyl-5,5'-di-tert-butyl-diphenylmethan 
• 801-19-4 3-Chlor-2,2'-dihydroxy-5,5'-di-tert-butyl-diphenylmethan 
• 2725-53-3 2-hydroxy-5-t-butylbenzaldehyde 
• 6638-87-5 4-(tert-butyl)-2-(hydroxymethyl)phenol 
• 799-13-3 bis(5-tert-butyl-2-hydroxyphenyl)methane 
• 475197-29-6 5-tertbutyl-3-[(5-tert-butyl)-2-hydroxy-3-(2-oxovinyl)benzyl]-2-hydroxybenz-aldehyde 
• 810-52-6 4-(tert-butyl)-2,6-bis{[5-(tert-butyl)-2-hydroxyphenyl]methyl}phenol 
• 1264-13-7 2,2'-Dihydroxy-5,5'-di-tert-butyl-3,3'-bis-(3-chlor-2-hydroxy-5-tert-butyl-benzyl)-diphenylmethan 
• 123765-91-3 C₄₃H₅₆O₄*2C₆H₁₂ 

Downstream Products

• 85097-22-9 3-<3-<3-<3-(Hydroxymethyl)-5-tert-butylsalicyl>-5-tert-butylsalicyl>-5-tert-butylsalicyl>-5-tert-butyl-2-hydroxybenzyl Alcohol 
• 117163-04-9 4-t-butyl-2-<2-acetoxy-5-t-butyl-3-<2-acetoxy-5-t-butyl-3-(2-acetoxy-5-t-butylbenzyl)benzyl>benzyl>phenyl acetate 
• 67988-30-1 2,2'-methylenebis<6-(2-hydroxybenzyl)phenol> 
• 917-51-1 C₆₅H₈₂Cl₂O₆ 
• 68803-63-4 3-<3-<3-(5-tert-butylsalicyl)-5-tert-butylsalicyl>-5-tert-butylsalicyl>-5-tert-butyl-2-hydroxybenzyl alcohol 
• 256510-69-7 4-tert-butyl-2-((5-(tert-butyl)-3-((5-tert-butyl)-2-hydroxyphenyl)methyl)-2-hydroxyphenyl)methyl-6-((5-tert-butyl)-2-hydroxy-3-(thienylmethyl)methyl)phenol 
• 340811-02-1 4-tert-butyl-2-((5-(tert-butyl)-3-((5-tert-butyl)-2-hydroxy-3-(hydroxymethyl)phenyl)methyl)-2-hydroxyphenyl)methyl-6-((5-tert-butyl)-2-hydroxy-3-(thienylmethyl)methyl)phenol 
• 149790-54-5 4-t-butyl-2-<2-acetoxy-5-t-butyl-3-<2-acetoxy-5-t-butyl-3-(2-acetoxy-5-t-butylbenzoyl)benzoyl>benzoyl>phenyl acetate 
• 72251-68-4 7,13,19,25-tetra-tert-butyl-2,3-dihomo-3-oxacalix[4]arene 
• 1407969-12-3 ethyl 5-(4-tert-butyl-2-(5-tert-butyl-2-(tert-butyldiphenylsilyloxy)benzyl)-6-(5-tert-butyl-3-(5-tert-butyl-2-(tert-butyldiphenylsilyloxy)benzyl)-2-hydroxybenzyl)phenoxy)pentanoate 
• 1407968-97-1 2-(3-(5-tert-butyl-2-(tert-butyldiphenylsilyloxy)benzyl)-5-tert-butyl-2-hydroxybenzyl)-6-(5-tert-butyl-2-(tert-butyldiphenylsilyloxy)benzyl)-4-tert-butylphenol 
• 1407968-96-0 2-(3-(5-tert-butyl-2-(tert-butyldiphenylsilyloxy)benzyl)-5-tert-butyl-2-hydroxybenzyl)-6-(5-tert-butyl-2-hydroxybenzyl)-4-tert-butylphenol 
• 1756-93-0 bis-{5-tert-butyl-3-[5-tert-butyl-3-(5-tert-butyl-2-hydroxy-benzyl)-2-hydroxy-benzyl]-2-hydroxy-phenyl}-methane 

Relevant academic research and scientific papers

Synthesis of Monofunctionalized Calix[5]arenes

Seven OH-free and O -permethylated monofunctionalized calix[5]arenes carrying either additional methyl or tert -butyl groups are prepared following fragment condensation protocols. This strategy proves to be superior to previous approaches. Calix[5]arenes with free OH groups all adopt a cone conformation stabilized by a seam of hydrogen bonds at the lower rim. Post-condensation modifications, i.e., methylation of phenolic OH groups or functional group interconversions can also be achieved. Bulky tert -butyl groups are also found to stabilize the cone conformations of O -methylated compounds. These compounds offer versatile functional groups that make these concave molecules interesting building blocks for the synthesis of more sophisticated molecular architectures.

Inclusion Properties of Acyclic p-Substituted Phenol-Formaldehyde Oligomers

Acyclic para-substituted phenol-formaldehyde oligomers (R=H, Me, n-Nu, t-Bu, and cyclohexyl; the number of phenol units=3-6) form host-guest complexes with various organic compounds.The inclusion property of the acyclic oligomers is greatly influenced by