Name | 4-Bromo-2,6-dichloroaniline |
Synonyms | 4-Bromo-2,6-dichloroaniline 2,6-DICHLORO-4-BROMOANILINE 4-BROMO-2,6-DICHLOROANILINE 4-Bromo-2,4,-dichloroaniline 4-BROMO-2,6-DICHLORO-BENZENAMINE 4-Bromo-2,6-dichloro-1-benzenamin (4-BROMO-2,6-DICHLOROPHENYL)AMINE 4-Bromo-2,6-dichloro-1-benzenamine (4-Bromo-2,6-dichlorophenyl)amine, 2,6-Dichloro-4-bromoaniline, 4-Bromo-2,6-dichloro-benzenamine |
CAS | 697-88-1 |
EINECS | 211-809-5 |
InChI | InChI=1/C6H4BrCl2N/c7-3-1-4(8)6(10)5(9)2-3/h1-2H,10H2 |
Molecular Formula | C6H4BrCl2N |
Molar Mass | 240.91 |
Density | 1.827±0.06 g/cm3(Predicted) |
Melting Point | 83-87 °C |
Boling Point | 256.5±35.0 °C(Predicted) |
Flash Point | 108.9°C |
Vapor Presure | 0.0153mmHg at 25°C |
Appearance | Crystalline powder |
BRN | 2089687 |
pKa | 0.00±0.10(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
Refractive Index | 1.648 |
MDL | MFCD00025162 |
Risk Codes | R22 - Harmful if swallowed R36/37/38 - Irritating to eyes, respiratory system and skin. R20/21/22 - Harmful by inhalation, in contact with skin and 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. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S22 - Do not breathe dust. |
WGK Germany | 3 |
HS Code | 29214200 |
Hazard Note | Irritant/Harmful |
Application | 4-bromo -2, 6-dichloroaniline is used to synthesize dipyard, Liguron, mikazolin and azo dyes, etc. Reagents for preparing 4-alkyl-1-phenylpyrazole and 4-alkyl-1-phenyltrioxo-octane derivatives of GABA receptor antagonist insecticides. |
Preparation | Using 2,6-dichloroaniline as raw material, NBS as brominating reagent, BPO as initiator, a free radical bromination reaction occurs in carbon tetrachloride solution to obtain 4-bromo-2, 6-dichloroaniline. 2,6-dichloroaniline, 30mL carbon tetrachloride, N-bromosuccinimide and benzoyl peroxide were added to the reaction system, reacted at 60 ℃ for 7h, and the reaction was monitored by TLC. After the reaction was completed, the solvent was distilled under reduced pressure. The obtained crude product was purified by column chromatography (V petroleum ether: V ethyl acetate = 10: 1) to obtain light yellow solid 1.20g. |