CAS 3466-32-8|4-Bromophenyl methyl sulfone
Introduction：Basic information about CAS 3466-32-8|4-Bromophenyl methyl sulfone, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | 4-Bromophenyl methyl sulfone | ||
|---|---|---|---|
| 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 | ChineseUSA | Flash Point | 164.6±25.7 °C |
Names
| Name | 1-bromo-4-methylsulfonylbenzene |
|---|---|
| Synonym | More Synonyms |
Chemical & Physical Properties
| Density | 1.6±0.1 g/cm3 |
|---|---|
| Boiling Point | 348.6±34.0 °C at 760 mmHg |
| Melting Point | 103-107 °C(lit.) |
| Molecular Formula | C7H7BrO2S |
| Molecular Weight | 235.098 |
| Flash Point | 164.6±25.7 °C |
| Exact Mass | 233.934998 |
| PSA | 42.52000 |
| LogP | 1.24 |
| Vapour Pressure | 0.0±0.7 mmHg at 25°C |
| Index of Refraction | 1.564 |
| InChIKey | FJLFSYRGFJDJMQ-UHFFFAOYSA-N |
| SMILES | CS(=O)(=O)c1ccc(Br)cc1 |
Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xn,Xi |
| Risk Phrases | R22 |
| Safety Phrases | S22-S24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2904909090 |
Customs
| HS Code | 2904909090 |
|---|---|
| Summary | HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0% |
Articles4
More Articles| 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 ... | |
| 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 cyc... | |
| 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 s... |
Synonyms
| Sulfone, p-bromophenyl methyl (8CI) |
| Sulfone,p-bromophenyl methyl |
| 1-bromo-4-methanesulfonyl-benzene |
| EINECS 222-421-0 |
| Benzene, 1-bromo-4- (methylsulfonyl)- |
| 1-Bromo-4-(methylsulfonyl)benzene |
| 4-MeO2SC6H4Br |
| Sulfone, p-bromophenyl methyl |
| 4-methanesulfonylbromobenzene |
| 4-bromophenyl methyl sulphone |
| Benzene, 1-bromo-4-(methylsulfonyl)- |
| 4-methylsulfonyl-bromobenzene |
| MFCD00025065 |
| p-methyl benzenesulfobromide |
| Methyl 4-bromophenyl sulfone |
| 4-Bromophenyl methyl sulfone |
| p-Bromophenyl methyl sulfone |
