701-69-9

Upstream product

• 874-63-5 3,5-dimethylmethoxybenzene 
• 55661-08-0 4-methoxy-2,6-dimethylbenzenesulfonyl chloride 

Downstream Products

• 55661-09-1 4-methoxy-2,6-dimethylphenyl methyl sulphide 
• 122443-59-8 4-nitrophenyl 2,6-dimethyl-4-methoxyphenyl sulfide 
• 122443-64-5 5-Methoxy-1,3-dimethyl-2-(4-nitro-benzenesulfonyl)-benzene 
• 14763-62-3 3,5-Dimethyl-4-methylmercapto-phenol 
• 61482-34-6 2-methanesulfonyl-5-methoxy-1,3-dimethyl-benzene 
• 214203-33-5 p-methoxybenzyl 3-(2,6-dimethyl-4-methoxyphenylthio)methyl-7-phenylacetamido-Δ3-cephem-4-carboxylate 
• 959640-91-6 tert-butyl {3-[(4-methoxy-2,6-dimethylphenyl)thio]propoxy}dimethylsilane 
• 959640-93-8 3-[(4-methoxy-2,6-dimethylphenyl)sulfonyl]butan-1-ol 
• 959640-95-0 {3-[(4-methoxy-2,6-dimethylphenyl)sulfonyl]butoxy}acetic acid 
• 959640-92-7 tert-butyl {3-[(4-methoxy-2,6-dimethylphenyl)sulfonyl]propoxy}dimethylsilane 
• 959640-94-9 tert-butyl {3-[(4-methoxy-2,6-dimethylphenyl)sulfonyl]butoxy}acetate 

Relevant academic research and scientific papers

Chemo- and product-selective electrooxidation of 3-(arylthiomethyl)- Δ3-cephems

Electrolysis of 3-arylthiomethyl-Δ3-cephems possessing various substituents on the arylthio moiety undergo chemo selective and product-selective electrooxidation to give several different products. These include isomeric mixtures of the corresponding methoxylated cephems, a bis[(Δ3-cephem-3-yl)methyl]disulfide or a 3-dimethoxymethyl- Δ3-cephem. The selectivity of the oxidation is highly dependent on the nature of the substituents on the arylthio moiety which suggests that both steric and electronic effects play an important role in the electrooxidation of 3-arylthiomethyl-Δ3-cephems.

ARYL SULFONES

Aryl sulfones of Formula (I) are provided, in which the variables are as described herein. Such compounds may be used to modulate bradykinin receptor activity in vivo or in vitro, and are particularly useful in the treatment of conditions responsive to B

SPIROCYCLIC SULFONAMIDES AND RELATED COMPOUNDS

Spirocyclic sulfonamides and related compounds of Formula 1 are provided : (Formula (I)): in which the variables are as described herein. Such compounds may be used to modulate bradykinin receptor activity in vivo or in vitro, and are particularly useful