| Identification | Back Directory | [Name]
2-Allyloxy-1,3,5-tribromobenzene | [CAS]
3278-89-5 | [Synonyms]
DXFR? 401
ALLYL TRIBROMOPHENYL ETHER
TRIBROMOPHENYL ALLYL ETHER
2-allyloxy-1,3,5-tribromobenzene
ALLYL 2,4,6-TRIBROMOPHENYL ETHER
2,4,6-Tribromophenyl allyl ether
1-(Allyloxy)-2,3,4-tribromobenzene
1,3,5-tribromo-2-prop-2-enoxybenzene
Allyl 2,4,6-tribromophenyl ether 98%
1,3,5-tribromo-2-prop-2-enoxy-benzene
1,3,5-tribromo-2-(2-propenyloxy)-benzen
Benzene,1,3,5-tribromo-2-(2-propenyloxy)
1,3,5-TRIBROMO-2-(2-PROPENYLOXY)-BENZENE
1,3,5-TribroMo-2-(2-propen-1-yloxy)-benzene
Benzene, 1,3,5-tribromo-2-(2-propen-1-yloxy)-
2,4,6-Tribromophenyl allyl ether @100 μg/mL in Toluene | [EINECS(EC#)]
221-913-2 | [Molecular Formula]
C9H7Br3O | [MDL Number]
MFCD00017773 | [MOL File]
3278-89-5.mol | [Molecular Weight]
370.86 |
| Chemical Properties | Back Directory | [Melting point ]
74-76 °C (lit.) | [Boiling point ]
339.5±37.0 °C(Predicted) | [density ]
1.950±0.06 g/cm3(Predicted) | [solubility ]
Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly) | [form ]
Solid | [color ]
Off-White to Beige | [InChI]
InChI=1S/C9H7Br3O/c1-2-3-13-9-7(11)4-6(10)5-8(9)12/h2,4-5H,1,3H2 | [InChIKey]
RZLLIOPGUFOWOD-UHFFFAOYSA-N | [SMILES]
C1(Br)=CC(Br)=CC(Br)=C1OCC=C | [EPA Substance Registry System]
Allyl 2,4,6-tribromophenyl ether (3278-89-5) |
| Hazard Information | Back Directory | [Application]
1,3,5-Tribromo-2-(2-propen-1-yloxy)-benzene is used as a brominated flame retardant.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package. | [Synthesis]
To the ethanol solution of the sodium tribromophenolate salt prepared in the step 1), the dispersing agent sodium stearate 2.5 g is added.And catalyst II phenyl triethyl ammonium chloride 5.6g,The temperature is raised to 75 ?? C to reflux the reaction.Further, 1000 ml of an ethanol solution of chloropropene having a volume ratio of chloropropene to ethanol of 1:5 was slowly added thereto, and then the reaction was kept at 75 ?? C for 6.5 h until the end.Then, the temperature is lowered to 7 ?? C in sequence, and then suction filtration is performed to recover the ethanol solution.After washing the filter cake with water, the filter cake was dried at 60 ?? C.2,4,6-Tribromophenyl allyl ether was obtained as a white powdery solid in a yield of 96.2%. |
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