39082-89-8

Upstream product

• 23905-47-7 bis-(3-acetylamino-phenyl)-disulfide 
• 626-01-7 3-Iodoaniline 
• 2524-78-9 N-(3-(methylthio)phenyl)acetamide 
• 1783-81-9 3-methylmercaptoaniline 
• 861377-83-5 acetic acid-(3-methanesulfinyl-anilide) 

Downstream Products

• 1783-81-9 3-methylmercaptoaniline 
• 1403818-86-9 N-(3-(methylsulfinyl)phenyl)-5-(thiophen-2-yl)-1H-pyrazolo[4,3-d]pyrimidin-7-amine 
• 1352310-80-5 C₂₅H₃₅NO₆S 
• 1352310-83-8 C₂₅H₃₅NO₆S 

Relevant academic research and scientific papers

Modulation of photochemical oxidation of thioethers to sulfoxides or sulfones using an aromatic ketone as the photocatalyst

We have developed an eco-friendly and chemo-selective photocatalytic synthesis of sulfoxides or sulfones via oxidation of sulfides (thioethers) at ambient temperature using air or O2 as the oxidant. An inexpensive thioxanthone was used as the photocatalyst. Our method offers excellent chemical yields and good functional group tolerance. The hydrogen bonding between hexafluoro-2-propanol (HFIP) and sulfoxides may play an important role in minimizing the over-oxidization of sulfoxides.

Kinase inhibitors (by machine translation)

The present invention relates to certain 4 - (substituted anilino) -2 - (substituted piperi -1 -yl) pyrimidine -5 - carboxamide compounds useful for the treatment or prevention of diseases or medical conditions mediated by signal transduction of CaMMK1 isotype. For example, such compounds and salts thereof may be used to treat or prevent a variety of different cancers. Diseases (including 2 diabetes) and/or immune-mediated diseases. (by machine translation)

BENZAMIDE COMPOUNDS AND RELATED METHODS OF USE

Benzamide compounds and derivatives thereof, as can be used for selective inhibition of the SIRT2 enzyme and/or therapeutic use in the treatment of Huntington's disease.

Benzodiazepine derivatives, compositions containing them and their use in therapy

Compounds of formula (I), and salts and prodrugs thereof wherein: R1 represents optionally substituted C? ??alkyl or C???cycloalkyl; R2 represents an optionally substituted phenyl or pyridyl group; R3 represents C??? alkyl or halo; R? represents C??? cycloalkyl; X is 0, 1, 2 or 3; are CCK and/or gastrin antagonists. They and compositions thereof are therefore useful in therapy.

Kinetics and Mechanism of Oxidation of Organic Sulphides by Lead Tetraacetate

Kinetics of oxidation of thirty-three organic sulphides, comprising monosubstituted aryl methyl sulphides and alkyl phenyl sulphides, by lead tetraacetate (LTA), to yield the corresponding sulphoxides, have been studied.The reaction is first order with re