219800-57-4

Basic information

• Product Name: 2-[3-[3-[3-(chloromethyl)-5-tert-butylsalicyl]-5-tert-butylsalicyl]-5-tert-butylsalicyl]-6-(chloromethyl)-4-tert-butylphenol
• Synonyms: 2-[3-[3-[3-(chloromethyl)-5-tert-butylsalicyl]-5-tert-butylsalicyl]-5-tert-butylsalicyl]-6-(chloromethyl)-4-tert-butylphenol
• CAS NO: 219800-57-4
• Molecular Weight: 733.859
• Mol File: 219800-57-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-[3-[3-[3-(chloromethyl)-5-tert-butylsalicyl]-5-tert-butylsalicyl]-5-tert-butylsalicyl]-6-(chloromethyl)-4-tert-butylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[3-[3-[3-(chloromethyl)-5-tert-butylsalicyl]-5-tert-butylsalicyl]-5-tert-butylsalicyl]-6-(chloromethyl)-4-tert-butylphenol(219800-57-4)
• EPA Substance Registry System: 2-[3-[3-[3-(chloromethyl)-5-tert-butylsalicyl]-5-tert-butylsalicyl]-5-tert-butylsalicyl]-6-(chloromethyl)-4-tert-butylphenol(219800-57-4)

Safety Data

• Hazardous Substances Data: 219800-57-4(Hazardous Substances Data)

Upstream product

• 85097-22-9 3-<3-<3-<3-(Hydroxymethyl)-5-tert-butylsalicyl>-5-tert-butylsalicyl>-5-tert-butylsalicyl>-5-tert-butyl-2-hydroxybenzyl Alcohol 

Relevant articles and documents

Facile syntheses of homothia- and homoazacalixarenes

Decahomotetrathiacalix[6]arenes were conveniently prepared from the 2:2 cyclization reactions of bis(chloromethyl)phenol-formaldehyde trimers with 1,2-ethanedithiol in high yields. In contrast, the similar reactions of the trimers with 1,3-propanedithiol

Syntheses of chiral calixarene analog incorporating amino acid residues: Molecular recognition for a racemic ammonium ion by the macrocycles

Chiral calixarene analog incorporating amino acid residues into macrocyclic rings was prepared. The macrocycles form a chiral concave, which is induced by the chiral transmission from the amino acid to the phenol-formaldehyde tetramer unit through the hyd