Basic information Safety Supplier Related

2-BROMO-4-IODOTOLUENE

Basic information Safety Supplier Related

2-BROMO-4-IODOTOLUENE Basic information

Product Name:
2-BROMO-4-IODOTOLUENE
Synonyms:
  • 2-BROMO-4-IODOTOLUENE
  • 2-bromo-4-iodo-1-methylbenzene
  • 1-BROMO-5-IODO-2-METHYLBENZENE
  • 1-Bromo-5-iodo-2-metnylbenzene
  • Benzene, 2-bromo-4-iodo-1-methyl-
  • 2-BROMO-4-IODOTOLUENE ISO 9001:2015 REACH
CAS:
26670-89-3
MF:
C7H6BrI
MW:
296.93
EINECS:
231-807-8
Product Categories:
  • Bromine Compounds
  • Iodine Compounds
Mol File:
26670-89-3.mol
More
Less

2-BROMO-4-IODOTOLUENE Chemical Properties

Melting point:
265-267℃
Boiling point:
263.6±28.0 °C(Predicted)
Density 
2.062
Flash point:
113℃
storage temp. 
Keep in dark place,Sealed in dry,2-8°C
Appearance
Colorless to light yellow Liquid
More
Less

Safety Information

HS Code 
2903998090
More
Less

2-BROMO-4-IODOTOLUENE Usage And Synthesis

Chemical Properties

off-white crystalline

Synthesis

7745-91-7

26670-89-3

(Synthesis of (2-1) 2-bromo-4-iodotoluene (0143): A mixed solution of 3-bromo-4-methylaniline (18.6 g, 0.1 mol) with 6 M hydrochloric acid (80 mL) was cooled to -5 °C and stirred under argon protection. An aqueous solution of sodium nitrite (15 mL, containing 7.35 g of sodium nitrite) was added slowly and dropwise while maintaining the reaction temperature below 0 °C. The reaction temperature was kept below 0 °C and the reaction temperature was kept below 0 °C. After the dropwise addition, the reaction mixture was continued to be stirred at -8 °C for 45 min. Subsequently, potassium iodide (33.2 g, 0.2 mol) was added in batches over a period of 3 hours while ensuring that the reaction temperature did not exceed 0 °C. The reaction mixture was then stirred at -8 °C for 45 min. After the addition was completed, the reaction mixture was allowed to warm up naturally to room temperature. At the end of the reaction, the reaction was quenched by the addition of 10% aqueous sodium bisulfite (50 mL) and then extracted with ether (3 × 50 mL). The organic layers were combined, washed with 10% aqueous sodium bisulfite (50 mL), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate = 20:1) to afford 2-bromo-4-iodotoluene (14.5 g, 49% yield).

References

[1] Patent: JP2018/90561, 2018, A. Location in patent: Paragraph 0087
[2] Photochemical and Photobiological Sciences, 2018, vol. 17, # 3, p. 290 - 301
[3] Patent: US2017/183291, 2017, A1. Location in patent: Paragraph 0142; 0143
[4] Patent: US5206235, 1993, A

2-BROMO-4-IODOTOLUENESupplier

Beijing dtftchem Technology Co., Ltd.
Tel
010-60275820 13031183356
Email
elainezt@sina.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Shijiazhuang Sdyano Fine Chemical Co., Ltd.
Tel
0311-89250318 031166536426
Email
master@sjzsdyn.com
Beijing Ouhe Technology Co., Ltd
Tel
010-010-82967028 13522913783
Email
2355560935@qq.com
JinYan Chemicals(ShangHai) Co.,Ltd.
Tel
13817811078
Email
sales@jingyan-chemical.com
More
Less

2-BROMO-4-IODOTOLUENE(26670-89-3)Related Product Information