84543-57-7

Upstream product

• 29392-46-9 ethyl thioformate 
• 35383-91-6 2,4,6-tri-tert-butylphenyllithium 

Downstream Products

• 89751-90-6 6,8-di-tert-butyl-3,4-dihydro-4,4-dimethyl-1H-2-benzothiine 
• 89738-85-2 C₄₆H₇₈S₂ 
• 92885-27-3 (3S,4S)-2-Methylene-3-methylsulfanyl-4-(2,4,6-tri-tert-butyl-phenyl)-thietane 
• 92885-26-2 (3S,4S)-3-tert-Butoxy-2-methylene-4-(2,4,6-tri-tert-butyl-phenyl)-thietane 
• 92885-30-8 (3S,4R)-2-Methylene-3-phenyl-4-(2,4,6-tri-tert-butyl-phenyl)-thietane 
• 92885-28-4 (3S,4S)-3-Ethylsulfanyl-2-methylene-4-(2,4,6-tri-tert-butyl-phenyl)-thietane 
• 92885-31-9 C₂₈H₃₇⁽²⁾HS 
• 89738-83-0 1,2-Bis-(2,4,6-tri-tert-butyl-phenyl)-ethane-1,2-dithiol 
• 89738-81-8 3,5-tri-t-butyl-2-(t-butylthiomethyl)benzene 
• 89738-82-9 1,3,5-Tri-tert-butyl-2-(1-tert-butylsulfanyl-2,2-dimethyl-propyl)-benzene 
• 176216-93-6 phenyl 2,4,6-tri-tert-butylbenzyl sulphide 
• 3975-81-3 2,4,6-tri(tert-butyl)benzaldehyde 
• 144424-50-0 2,2-diphenyl-3-(2,4,6-tri-t-butylphenyl)thiirane 
• 17799-08-5 4,6-Di-tert-butyl-1,1-dimethyl-indan 

Relevant academic research and scientific papers

Synthesis, Structure, and Some Reactions of (2,4,6-Tri-t-butyl)thiobenzaldehyde, the First Stable Aromatic Thioaldehyde

The title compound 1 was synthesized by the reaction of 2,4,6-tri-t-butylphenyllithium with O-ethyl thioformate or that of 2,4,6-tri-t-butylbenzaldehyde hydrazone with disulfur dichloride in the presence of triethylamine. The thioaldehyde 1 is a purple cr

Synthesis of 2,4,6-Tri-t-butylthiobenzaldehyde, the First Stable Thiobenzaldehyde

The title compound, an extremely stable thiobenzaldehyde, was prepared by the reaction of 2,4,6-tri-t-butylphenyl-lithium with O-ethyl thioformate or the reaction of 2,4,6-tri-t-butylbenzaldehyde hydrazone with disulphur dichloride.