846567-82-6

Upstream product

• 77-78-1 dimethyl sulfate 
• 846567-81-5 ethyl 3-bromo-2-hydroxy-6-methylbenzoate 
• 20717-15-1 3-ethyl-6-methyl-2-hydroxybenzoic acid 

Downstream Products

• 1286176-85-9 6-(benzenesulphonylmethyl)-2-methoxy-3-propylbenzoic acid 
• 1286178-88-8 ethyl 6-(benzenesulphonylmethyl)-2-methoxy-3-propylbenzoate 
• 1286178-57-1 6-(benzenesulphonylmethyl)-2-[2-(t-butoxycarbonyl)aminoethoxy]-3-(furan-3-yl)benzoic acid 
• 1286177-37-4 6-(benzenesulphonylmethyl)-3-(isoxazol-3-yl)-2-methoxybenzoic acid 
• 1286179-26-7 ethyl 6-(benzenesulphonylmethyl)-3-(isoxazol-3-yl)-2-methoxybenzoate 
• 1286179-87-0 ethyl 3-bromo-6-(4-fluorobenzenesulphonylmethyl)-2-methoxybenzoate 
• 1286179-85-8 ethyl 6-(4-chlorobenzenesulphonylmethyl)-3-bromo-2-methoxybenzoate 
• 1286179-90-5 ethyl 3-bromo-6-(bromomethyl)-2-methoxybenzoate 
• 1286179-92-7 ethyl 3-bromo-6-(dibromomethyl)-2-methoxybenzoate 
• 1286179-69-8 ethyl 3-bromo-6-(phenylthiomethyl)-2-methoxybenzoate 
• 1286179-42-7 ethyl 3-acetyl-6-(benzenesulphonylmethyl)-2-methoxybenzoate 
• 1286179-29-0 ethyl 6-(benzenesulphonylmethyl)-3-(5-hydroxy-4,5-dihydroisoxazol-3-yl)-2-methoxybenzoate 
• 1286179-34-7 ethyl 6-(benzenesulphonylmethyl)-3-bromo-2-hydroxybenzoate 
• 1286178-98-0 ethyl 6-(benzenesulphonylmethyl)-2-methoxy-3-(oxazol-5-yl)benzoate 

Relevant academic research and scientific papers

SULPHONE COMPOUNDS AND METHODS OF MAKING AND USING SAME

The invention provides sulphone compounds and their use in treating medical disorders, such as obesity. Pharmaceutical compositions and methods of making various sulphone compounds are provided. The compounds are contemplated to have activity against methionyl aminopeptidase 2

A novel synthesis of bromomethoxy disubstituted derivatives of benzocyclobutenone

Flash vacuum pyrolysis of ortho-methyl aromatic acid chlorides has been used to prepare a variety of substituted derivatives of the benzocyclobutenone ring system starting from simple precursors. The significance of the present reaction lies in the fact that the bromine atom present in the aromatic nucleus, remains undisturbed during the high temperature treatment employed in the pyrolysis and forms, a bromomethoxyketone successfully. This is an altogether new approach.