Basic information Safety Supplier Related

5,6-DICHLORO-2-METHYLBENZIMIDAZOLE

Basic information Safety Supplier Related

5,6-DICHLORO-2-METHYLBENZIMIDAZOLE Basic information

Product Name:
5,6-DICHLORO-2-METHYLBENZIMIDAZOLE
Synonyms:
  • 5,6-DICHLORO-2-METHYL-1H-BENZIMIDAZOLE
  • 5,6-DICHLORO-2-METHYL-1H-BENZO[D]IMIDAZOLE
  • 5,6-DICHLORO-2-METHYLBENZIMIDAZOLE
  • BUTTPARK 147\15-46
  • 5,6-Dichloro-2-methylbenzoimidazole
  • 5,6-dichloro-2-Methyl-1H-1,3-benzodiazole
  • 5,6-Dichloro-2-methylbenzimidazole>
  • 1H-Benzimidazole, 5,6-dichloro-2-methyl-
CAS:
6478-79-1
MF:
C8H6Cl2N2
MW:
201.05
Product Categories:
  • Imidazol&Benzimidazole
  • Aromatics
  • Heterocycles
  • Intermediates
Mol File:
6478-79-1.mol
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5,6-DICHLORO-2-METHYLBENZIMIDAZOLE Chemical Properties

Melting point:
238-240
Boiling point:
409.0±25.0 °C(Predicted)
Density 
1.486
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
pka
9.94±0.10(Predicted)
color 
White to Orange to Green
CAS DataBase Reference
6478-79-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2933998090
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5,6-DICHLORO-2-METHYLBENZIMIDAZOLE Usage And Synthesis

Uses

5,6-Dichloro-2-methylbenzimidazole is a benzimidazole with antiparasitic activity. It also shows aminopyrine demethylase-inhibiting activity.

Synthesis

5348-42-5

141-97-9

6478-79-1

GENERAL METHOD: A mixture of 4,5-dichloro-1,2-phenylenediamine (200 mg, 1.85 mmol) and ethyl acetoacetate (722 mg, 5.55 mmol) was added with GdCl3-6H2O (25 mg, 0.09 mmol), and the reaction mixture was stirred for 3.0 hours at 80 °C. After completion of the reaction (monitored by TLC), the reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 5,6-dichloro-2-methylbenzimidazole crude. The crude product was further purified by column chromatography with the eluent being a hexane solution of 10% ethyl acetate.

References

[1] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2015, vol. 54B, # 8, p. 953 - 957

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