84654-55-7

Upstream product

• 64-17-5 ethanol 
• 1988-88-1 2,6-di-tert-butyl-4-cyanophenol 

Downstream Products

• 105648-49-5 2,4,6-tris(3,5-di-t-butyl-4-oxyphenyl)-s-triazine 
• 114811-88-0 2-amino-4-(4-hydroxy-3,5-di-tert-butylphenyl)-6-<β-(4-hydroxy-3,5-di-tert-butylphenyl)ethyl>-sym-triazine 
• 92176-17-5 2-(4-Hydroxy-3,5-di-tert-butylphenyl)-Δ²-oxazoline 
• 3203-02-9 4-(1H-benz[d]imidazol-2-yl)-2,6-di-tert-butylphenol 
• 3202-91-3 2-(4-Hydroxy-3,5-di-tert-butylphenyl)benzoxazole 
• 3202-95-7 2,6-di-tert-butyl-4-(5-phenyl-[1,3,4]oxadiazol-2-yl)-phenol 
• 1605320-76-0 O,O,O,O-tetra(trimethylsilyl)-1-amino-1-(3,5-di-tert-butyl-4-hydroxyphenyl)methylenediphosphonate 
• 1605320-77-1 1-amino-1-(3,5-di-tert-butyl-4-hydroxyphenyl)-methylenediphosphonic acid 

Relevant academic research and scientific papers

SYNTHESIS AND PROPERTIES OF symm-TRIAZINE DERIVATIVES. 4.* SYNTHESIS OF 2,4,6-TRISUBSTITUTED symm-TRIAZINES CONTAINING STERICALLY-HINDERED PHENOL FRAGMENTS

2,4,6-Trisubstituted symm-triazines containing sterically-hindered phenol fragments were synthesized by the cyclotrimerization of ethyl iminoesters. 2,4,6-Trimercapto-symm-triazine derivatives containing shielded phenol residues may be formed by the cyclo