| Identification | Back Directory | [Name]
3,5-DIBROMOSULFANILAMIDE | [CAS]
39150-45-3 | [Synonyms]
dibromosulfanilamide
3,5-DIBROMOSULFANILAMIDE
2,6-dibromosulfanilamide
3,5-DIBROMOSULPHANILAMIDE
3,5-DIBROMOSULPHANILAMIDE 80%
3,5-DIBROMOSULFANILAMIDE 97+%
3,5-DIBROMOSULFANILAMIDE: TECH., 80%
4-Amino-3,5-dibromobenzenesulfonamide
3,5-Dibromo-4-aminobenzenesulfonamide
4-Amino-3,5-dibromobenzenesulphonamide
Benzenesulfonamide, 4-amino-3,5-dibromo- | [EINECS(EC#)]
254-321-8 | [Molecular Formula]
C6H6Br2N2O2S | [MDL Number]
MFCD00014783 | [MOL File]
39150-45-3.mol | [Molecular Weight]
330 |
| Chemical Properties | Back Directory | [Melting point ]
235-237°C | [Boiling point ]
458.2±55.0 °C(Predicted) | [density ]
2.156±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
powder to crystal | [pka]
9.57±0.60(Predicted) | [color ]
White to Light yellow to Light orange |
| Hazard Information | Back Directory | [Chemical Properties]
White crystals, melting point 236-238℃. | [Synthesis]
Fifty grams (0.29 mole) of sulfanilamide is dissolved in a mixture of 850 ml. of water and 100 ml. (0.68 mole) of 40% hydrobromic acid. The solution is heated as above but to 70–75° and 65 g. (59 ml., 0.58 mole) of 30% hydrogen peroxide is added. A precipitate settles in 2–3 minutes, and the solution becomes yellow. The heat of the reaction causes the internal temperature to rise without further application of heat to a maximum of 85–90℃ after 10 minutes; by the end of the reaction time, the temperature will have fallen to about 70℃. After a total reaction time of 30 minutes, when the mixture has become almost solid and is very difficult to stir, the material is filtered hot. The yield of 3,5-dibromosulfanilamide is 85–90 g (90–94%), and the crude tan product melts over a range of 1–2° in the region 230–237℃.
| [References]
[1] Green Chemistry, 2011, vol. 13, # 8, p. 2187 - 2196
[2] European Journal of Medicinal Chemistry, 2016, vol. 124, p. 229 - 236
[3] Analytical Chemistry, 1984, vol. 56, # 12, p. 2157 - 2160
[4] Organic Syntheses, 1955, vol. Coll. Vol. III, p. 262
[5] Gazzetta Chimica Italiana, 1948, vol. 78, p. 275,280 |
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