Name | 2,5-Dibromo-3,4-dinitrothiophene |
Synonyms | S1073 NSC 84661 AKOS 92299 DibroMo-3,4-dinitrothio 2,5-Dibromo-3,4-dinitrthiphene 2,5-DIBROMO-3,4-DINITROTHIOPHENE 2,5-Dibromo-3,4-dinitrothiophene |
CAS | 52431-30-8 |
EINECS | 676-535-4 |
InChI | InChI=1/C4Br2N2O4S/c5-3-1(7(9)10)2(8(11)12)4(6)13-3 |
InChIKey | AHGHPBPARMANQD-UHFFFAOYSA-N |
Molecular Formula | C4Br2N2O4S |
Molar Mass | 331.93 |
Density | 2.459±0.06 g/cm3(Predicted) |
Melting Point | 137°C |
Boling Point | 341.2±37.0 °C(Predicted) |
Flash Point | 160.2°C |
Water Solubility | Insoluble in water. |
Solubility | Acetone, Methanol |
Vapor Presure | 0.000161mmHg at 25°C |
Appearance | Solid |
Color | Light Orange |
BRN | 218219 |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
Refractive Index | 1.716 |
MDL | MFCD00015537 |
Hazard Symbols | Xn - Harmful |
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R22 - Harmful if swallowed |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S37 - Wear suitable gloves. |
WGK Germany | 3 |
HS Code | 29349990 |
Use | 2,5-dibromo-3, 4-dinitrothiophene is an organic intermediate. 2, 5-dibromo-3, 4-dinitrothiophene can be used to prepare 2, 5-dibromo-3, 4-diaminothiophene, 2, 5-dibromo-3, 4-diaminothiophene is an antibacterial chain extender. |
preparation | the first step can be obtained by one-step nitration of 2, 5-dibromothiophene: 5mL concentrated sulfuric acid and 5mL fuming sulfuric acid are mixed evenly in a three-mouth flask, then 1mL 2,5-dibromothiophene is added dropwise into the mixed acid, stirred for 30min, cooled down in an ice bath, controlled the temperature below 20 ℃, and the stirring speed is 100r/min; step 2: add 3mL of concentrated nitric acid dropwise to the system under stirring and stir for 5 hours. the reaction process requires ice bath to cool down, control the temperature below 30 ℃, and stir at a speed of 100r /min; Step 3: Pour the reaction product into 300g ice cubes and stir until the ice cubes are completely melted; Then vacuum suction filtration is carried out, and the obtained solid is fully washed and filtered with water. Then recrystallized with methanol and the solid is precipitated, the solution was removed by suction filtration, and 2, 5-dibromo-3, 4-dinitrothiophene was obtained after drying. |