153872-76-5

Upstream product

• 1138-52-9 3,5-Di-tert-butylphenol 

Downstream Products

• 202060-91-1 1,5-di-t-butyl-2-bromo-3-isopropoxybenzene 
• 97391-27-0 2,4-di-tert-butyl-6-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 1138-52-9 3,5-Di-tert-butylphenol 
• 1334501-47-1 (2-bromo-3,5-di-tert-butylphenoxy)triisopropylsilane 
• 153872-77-6 2-bromo-1,5-di-tert-butyl-3-methoxybenzene 
• 1848244-75-6 dicyclohexyl(2',4'-di-tert-butyl-6'-methoxy-[1,1'-biphenyl]-2-yl)phosphane 
• 153872-85-6 2,4-di-t-butyl-6-methoxyphenyldithioxophosphorane 
• 153872-78-7 C₁₅H₂₃Cl₂OP 
• 153872-81-2 2,4-di-t-butyl-6-methoxyphenylphosphine 

Relevant academic research and scientific papers

N-substituted aminotriphenylphosphonium tribromides as novel brominating agents

A number of N-substituted aminotriphenylphosphonium tribromides were investigated for their brominating ability of substituted phenols. It was found that t-butylaminotriphenylphosphonium tribromide, I, exhibits a good and a rather high regiospecificity in comparison with the commonly used bromine.

An Improved System for the Aqueous Lipshutz-Negishi Cross-Coupling of Alkyl Halides with Aryl Electrophiles

The development of a palladacyclic precatalyst supported by a new biaryl(dialkyl)phosphine ligand (VPhos) in combination with octanoic acid/sodium octanoate as a simple and effective surfactant system provided an improved catalyst system for the rapid con

An active ferrocenyl triarylphosphine for palladium-catalyzed Suzuki-Miyaura cross-coupling of aryl halides

Pd-catalyzed Suzuki-Miyaura reaction of aryl chlorides was accomplished through the use of an active ferrocene-based triarylphosphine ligand. This air- and moisture-stable ligand was found to be effective for the cross-coupling of aryl halides at room temperature to 115 °C.

Base and cation effects on the suzuki cross-coupling of bulky arylboronic acid with halopyridines: Synthesis of pyridylphenols

Strong base and large size cation have been shown to accelerate the rate and the yield of Suzuki coupling of a sterically bulky boronic acid with halopyridines in DME for the synthesis of pyridylphenols.

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