153872-85-6

Upstream product

• 153872-78-7 C₁₅H₂₃Cl₂OP 
• 153872-77-6 2-bromo-1,5-di-tert-butyl-3-methoxybenzene 
• 153872-76-5 2-bromo-3,5-di-tert-butylphenol 
• 1138-52-9 3,5-Di-tert-butylphenol 
• 153872-81-2 2,4-di-t-butyl-6-methoxyphenylphosphine 

Downstream Products

• 1450-31-3 Thiobenzophenon 

Relevant academic research and scientific papers

2,4-Di-t-butyl-6-methoxyphenyldithioxophosphorane as a Probe for the Mechanistic Studies of Lawesson's Reagent

The chemical conversion of carbonyl to thiocarbonyl compound was directly achieved by the treatment of benzophenone with 2,4-do-t-butyl-6-methoxyphenyldithioxophosphorane, which was prepared by the thermolysis of the corresponding dimeric species, 1,3,2,4-dithiadiphosphetane 2,4-disulfides.

New type of phosphorus compounds containing sulfur and selenium

New type of phosphorus compounds containing the P=S or P=Se groups were prepared by utilization of sterically protecting group carrying amino groups with the aid of intramolecular coordination effect.

Preparations and Sulfurization Reactions of (2,4-Di-t-butyl-6-methoxyphenyl)phosphine and 1-(2,4-Di-t-butyl-6-methoxyphenyl)-2-(2,4,6-tri-t-butylphenyl)diphosphene

A phosphonous dichloride carrying 2,4-di-t-butyl-6-methoxyphenyl as a novel sterically protecting group was prepared and converted to an unsymmetrical diphosphene, which reacted with sulfur to give the corresponding diphosphene sulfide and thiadiphosphira