| Identification | More | [Name]
1-BROMO-2,4-DICHLOROBENZENE | [CAS]
1193-72-2 | [Synonyms]
1-BROMO-2,4-DICHLOROBENZENE
2,4-DICHLOROBROMOBENZENE
BROMO(2-)-4-DICHLOROBENZENE
Benzene, 1-bromo-2,4-dichloro-
2,4-Dichloro Bromo Benzene 4'-Phenyl Acetophenone
1-Bromo-2,4-dichlorobenzene, 98+%
1-BROMO-2,4-DICHLOROBENZENE/2,4-DICHLOROBROMOBENZENE | [EINECS(EC#)]
214-778-6 | [Molecular Formula]
C6H3BrCl2 | [MDL Number]
MFCD00018333 | [Molecular Weight]
225.9 | [MOL File]
1193-72-2.mol |
| Chemical Properties | Back Directory | [Appearance]
colorless to light yellow crystalline mass or | [Melting point ]
26-30 °C(lit.)
| [Boiling point ]
235°C | [density ]
1,89 g/cm3 | [refractive index ]
1.5700 (estimate) | [Fp ]
>230 °F
| [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
powder to lump to clear liquid | [color ]
White or Colorless to Light yellow | [Water Solubility ]
Slightly soluble in water. | [BRN ]
1635733 | [CAS DataBase Reference]
1193-72-2(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection . | [RIDADR ]
UN 2810 6.1/PG 1
| [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29039990 |
| Hazard Information | Back Directory | [Chemical Properties]
colorless to light yellow crystalline mass or | [Uses]
1-Bromo-2,4-dichlorobenzene is used to produce 2,4,4'-trichloro-biphenyl. This reaction will need aq. Na2CO3 and solvents dioxane, ethanol. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields. | [General Description]
1-Bromo-2,4-dichlorobenzene is an aryl halide. It can be distinguished from the other bromodichlorobenzene isomers using IR and Raman spectral data. It can undergo Suzuki–Miyaura cross-coupling reaction with arylboronic acids in the presence of different Suzuki catalysts. |
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