94008-86-3

Upstream product

• 137-06-4 2-thiocresol 
• 89-98-5 2-chloro-benzaldehyde 

Downstream Products

• 94008-81-8 1-phenyl-1-<2-(2-methylphenylphenylthio)phenyl>methanol 
• 72731-28-3 1-Methyl-9-pentafluorophenyl-9H-thioxanthene 10,10-dioxide 
• 94008-84-1 (9R,10R)-1-Methyl-9-pentafluorophenyl-9H-thioxanthene 10-oxide 
• 72731-22-7 (9R,10R)-4-Methyl-9-(2,3,5,6-tetramethyl-phenyl)-9H-thioxanthene 10-oxide 
• 72731-19-2 (9R,10S)-4-Methyl-9-phenyl-9H-thioxanthene 10-oxide 
• 91127-79-6 1-methyl-9-(pentafluorophenyl)thioxanthene 
• 91127-80-9 4-methyl-9-(2,3,5,6-tetramethylphenyl)thioxanthene 
• 91127-77-4 4-methyl-9-phenylthioxanthene 
• 94008-83-0 1-<2-(2-methylphenylthio)phenyl>-1-pentafluorophenylmethanol 
• 94008-82-9 1-<2-(2-methylphenylthio)phenyl>-1-(2,3,5,6-tetramethylphenyl)methanol 

Relevant academic research and scientific papers

A concise synthesis of ortho-substituted aryl-acrylamides - Potent activators of soluble guanylyl cyclase

Horner-Emmons reaction of phosphonate amides with aldehydes leads to generation of o-substituted aryl-acrylamides. These compounds have been shown to be useful to quickly establish structure-activity relationships (SAR) for soluble guanylyl cyclase (sGC)

Stereochemistry of 9-Arylthioxanthene 10-Oxides and 10,10-Dioxides

The stereochemistry of 9-arylthioxanthene 10-oxides and 10,10-dioxides was determined by detailed investigation of the 1H-NMR spectra.These sulfoxides and sulfones were synthesized by oxidation of the corresponding 9-arylthioxanthenes with m-ch