Basic information Safety Supplier Related

1,4-DIBROMO-2,3,5,6-TETRAMETHYLBENZENE

Basic information Safety Supplier Related

1,4-DIBROMO-2,3,5,6-TETRAMETHYLBENZENE Basic information

Product Name:
1,4-DIBROMO-2,3,5,6-TETRAMETHYLBENZENE
Synonyms:
  • 1,4-DIBROMO-2,3,5,6-TETRAMETHYLBENZENE
  • 1,2,4,5-Tetramethyl-3,6-dibromobenzene
  • 2,3,5,6-Tetramethyl-1,4-phenylene dibromide
  • Dibromodurene
  • 3,6-Dibromodurene
  • Benzene,1,4-dibroMo-2,3,5,6-tetraMethyl-
  • 1,4-Dibromotetramethylbenzene
  • 4,6-Dibromo-1,2,4,5-tetramethylbenzene
CAS:
1646-54-4
MF:
C10H12Br2
MW:
292.01
Mol File:
1646-54-4.mol
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1,4-DIBROMO-2,3,5,6-TETRAMETHYLBENZENE Chemical Properties

Melting point:
202-204 °C
Boiling point:
307.7±37.0 °C(Predicted)
Density 
1.562±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Toluene
form 
powder to crystal
color 
White to Almost white
EPA Substance Registry System
Benzene, 1,4-dibromo-2,3,5,6-tetramethyl- (1646-54-4)
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Safety Information

HS Code 
2903.99.8001
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1,4-DIBROMO-2,3,5,6-TETRAMETHYLBENZENE Usage And Synthesis

Synthesis

95-93-2

1646-54-4

1. 1,2,4,5-tetramethylbenzene (25.0 g, 0.18 mol) and 150 mL of methylene chloride were added to a dry three-necked flask with stirring until completely dissolved. 2. Iodine (I2, 1.0 g, 3.94 mmol) was added to the solution as a catalyst. 3. Under stirring, bromine (Br2, 24 mL, 74.6 g, 0.47 mol) dissolved in a 100 mL of dichloromethane. 4. After the dropwise addition was completed, the reaction mixture was heated to reflux and held for 1.5 h. 5. After the reaction was completed, it was cooled to room temperature and the reaction was quenched by the addition of 5 M aqueous sodium hydroxide (50 mL). 6. The solid product was collected by filtration, washed with deionized water, and dried to afford 1,4-dibromo-2,3,5,6-tetramethylbenzene in 93% yield ( The product was characterized by 1H NMR (500 MHz, CDCl3) and 13C NMR (125.68 MHz, CDCl3): 1H NMR δ 2.48 (s, 12H); 13C NMR δ 135.2, 128.3, 22.4. 8. The 1H NMR spectrum and structure of the product are shown in Figure 1.

References

[1] Patent: KR2015/112649, 2015, A. Location in patent: Paragraph 0110-0112
[2] Patent: US2011/130593, 2011, A1. Location in patent: Page/Page column 6
[3] Angewandte Chemie - International Edition, 2016, vol. 55, # 9, p. 3049 - 3053
[4] Angew. Chem., 2016, vol. 128, # 9, p. 3101 - 3105,5
[5] Bulletin of the Chemical Society of Japan, 1989, vol. 62, # 2, p. 439 - 443

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