4-Bromophenyl methyl sulfone
4-Bromophenyl methyl sulfone structure
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Common Name | 4-Bromophenyl methyl sulfone | ||
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| CAS Number | 3466-32-8 | Molecular Weight | 235.098 | |
| Density | 1.6±0.1 g/cm3 | Boiling Point | 348.6±34.0 °C at 760 mmHg | |
| Molecular Formula | C7H7BrO2S | Melting Point | 103-107 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 164.6±25.7 °C | |
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Cerebrovasodilatation through selective inhibition of the enzyme carbonic anhydrase. 3. 5-(Arylthio)-, 5-(arylsulfinyl)-, and 5-(arylsulfonyl)thiophene-2-sulfonamides.
J. Med. Chem. 24(8) , 959-64, (1981) A series of 5-(arylthio)-, 5-(arylsulfinyl)-, and 5-(arylsulfonyl)thiophene-2-sulfonamides is described and anticonvulsant activities are listed for the compounds. In most cases, the sulfones had the highest activity and the sulfides the least. Sulfones with ... |
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Efficient green-light-emitting electrochemical cells based on ionic iridium complexes with sulfone-containing cyclometalating ligands.
Chemistry 19(26) , 8597-609, (2013) A new approach to obtain green-emitting iridium(III) complexes is described. The synthetic approach consists of introducing a methylsulfone electron-withdrawing substituent into a 4-phenylpyrazole cyclometalating ligand in order to stabilize the highest-occup... |
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Phenoxyphenyl sulfone N-formylhydroxylamines (retrohydroxamates) as potent, selective, orally bioavailable matrix metalloproteinase inhibitors.
J. Med. Chem. 45(1) , 219-32, (2002) A novel series of sulfone N-formylhydroxylamines (retrohydroxamates) have been investigated as matrix metalloproteinases (MMP) inhibitors. The substitution of the ether linkage of ABT-770 (5) with a sulfone group 13a led to a substantial increase in activity ... |
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Cooperativity and steric hindrance: important factors in the binding of a-cyclodextrin with para-substituted aryl alkyl sulfides, sulfoxides and sulfones. Davies DM and Deary ME.
J. Chem. Soc., Perkin Trans. II 7 , 1287-1294, (1995)
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