213135-33-2

Upstream product

• 141938-37-6 (3,5-dibromophenyl)(methyl)sulfane 
• 1435-51-4 1,3-dibromo-5-fluorobenzene 
• 626-39-1 1,3,5-trisbromobenzene 
• 213135-32-1 1-Methylsulfanyl-3,5-bis-p-tolylsulfanyl-benzene 

Downstream Products

• 1443155-56-3 C₄₀H₂₈N₂S₃ 
• 1443155-53-0 C₂₆H₂₀Br₂S₃ 
• 213135-34-3 C₄₇H₄₀S₇ 

Relevant academic research and scientific papers

Efficient formation of aromatic thiols from thiomethylated precursors

As a model study, a series of linear and branched p-phenylene and m- phenylene sulfides, functionalized by a thiomethyl group, were deprotected to thiols while using various alkyl thiolates at 160°C in DMF. Many complex aromatic thiols were obtained in al

Polysulfurated branched molecules containing functionalized m-phenylene sulfides

Polysulfurated branched molecules (dendrons) containing functionalized m-phenylene sulfide units were synthesized. An efficient way of making complex aromatic thiols from arylmethylthio groups is shown. A systematic study of the selectivity for producing a new series of phenylene sulfides was achieved. It has lead to the synthesis of rare dendrons containing sulfur and it will open the door to new poly(arylthio) dendrimers.