20904-31-8

Upstream product

• 636-98-6 p-nitrobenzene iodide 
• 4892-02-8 Methyl thiosalicylate 
• 1849-36-1 para-nitrobenzenethiol 
• 100-00-5 4-chlorobenzonitrile 
• 67-56-1 methanol 
• 20904-30-7 2-((4-nitrophenyl)thio)benzoic acid 

Downstream Products

• 20904-33-0 4,4'-Bis-(2-hydroxymethyl-phenyl-mercapto)-azoxybenzol 
• 20904-43-2 2-(4-Amino-phenylmercapto)-benzoesaeure-methylester 
• 16174-93-9 2-(4-Nitro-phenylmercapto)-benzylalkohol 
• 934670-77-6 2-((4-aminophenyl)thio)-N-(2-methoxyphenyl)benzamide 
• 16174-96-2 2-(4-Nitro-phenylmercapto)-phenylessigsaeure 
• 16174-95-1 2-(4-Nitro-phenylmercapto)-phenyl-acetonitril 
• 16174-94-0 2-(4-Nitro-phenylmercapto)-benzylchlorid 
• 20904-44-3 2-(4-Amino-phenylmercapto)-benzylalkohol 
• 20904-30-7 2-((4-nitrophenyl)thio)benzoic acid 

Relevant academic research and scientific papers

CONFORMATION OF DIARYL SULPHIDES WITH INTRAMOLECULAR SULPHUR(II)-OXYGEN INTERACTION: AN X-RAY STUDY OF METHYL 2-(4-NITROPHENYLTHIO)BENZOATE AND 2-DIAZOACETYL-4'-NITRODIPHENYL SULPHIDE

The molecular structures of methyl 2-(4-nitrophenylthio)benzoate and 2-diazoacetyl-4'-nitrodiphenyl sulphide have been determined by X-ray diffraction.The skew conformation observed for the ester is favourable to the formation of a sulphur(II)-oxigen(carb

Coupling of thiols and aromatic halides promoted by diboron derived super electron donors

We have proven that pyridine-boryl complexes can be used as superelectron donors to promote the coupling of thiols and aromatic halides through a SRN1 mechanism. The reaction is efficient for a broad substrate scope, tolerating heterocycles including pyridines, enolizable or reducible functional groups. The method has been applied to intermediates in drug synthesis as well as interesting functionalized polythioethers through a controlled and consecutive intramolecular electron transfer process.

Synthesis and structure-activity relationship studies of hiv-1 virion infectivity factor (vif) inhibitors that block viral replication

The human immunodeficiency virus1 (HIV-1) virion infectivity factor (Vif) protein, essential for in vivo viral replication, protects the virus from innate antiviral cellular factor apolipoproteinB mRNA-editing, enzyme-catalytic, polypeptide-like3G (APOBEC

Composition and synthesis of new reagents for inhibition of HIV replication

The present invention provides compounds and compositions for inhibiting Vif and methods for treating viral infection, e.g., HIV infection.