Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Chemical pesticides >  Germicide >  Azole fungicides >  5-IODO-2-METHYLBENZIMIDAZOLE

5-IODO-2-METHYLBENZIMIDAZOLE

Basic information Safety Supplier Related

5-IODO-2-METHYLBENZIMIDAZOLE Basic information

Product Name:
5-IODO-2-METHYLBENZIMIDAZOLE
Synonyms:
  • 5-IODO-2-METHYLBENZIMIDAZOLE
  • 5-Iodo-2-methyl-1H-benzimidazole
  • 5-iodo-2-Methyl-1H-benzo[d]iMidazole
  • 1H-Benzimidazole,6-iodo-2-methyl-
  • 6-iodo-2-methyl-1H-benzimidazole
  • 5(6)-IODO-2-METHYL BENZIMIDAZOLE
CAS:
2818-70-4
MF:
C8H7IN2
MW:
258.06
Mol File:
2818-70-4.mol
More
Less

5-IODO-2-METHYLBENZIMIDAZOLE Chemical Properties

Melting point:
220 °C
Boiling point:
419.4±18.0 °C(Predicted)
Density 
1.933±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
10.65±0.10(Predicted)
Appearance
Light brown to brown Solid
More
Less

Safety Information

Hazard Codes 
Xi
Risk Statements 
41
Safety Statements 
26-39
HS Code 
2933998090
More
Less

5-IODO-2-METHYLBENZIMIDAZOLE Usage And Synthesis

Synthesis

1445-45-0

20691-72-9

615-15-6

2818-70-4

GENERAL METHOD: 4-Iodo-2-nitroaniline (1 mmol) was mixed with indium powder (574 mg, 5.0 mmol) and acetic acid (0.572 mL, 10 mmol) in ethyl acetate (2 mL). Subsequently, a solution of ethyl acetate (3 mL for 2-nitroaniline; 8 mL for 1,2-dinitroaromatics) of trimethyl orthoacetate (2.0 mmol) was added. The reaction mixture was heated to reflux and stirred under nitrogen protection. Upon completion of the reaction, the reaction mixture was diluted with ethyl acetate (30 mL), filtered through diatomaceous earth and the filtrate was poured into 10% NaHCO3 solution (30 mL). The aqueous phase was extracted with ethyl acetate (30 mL x 3), the organic phases were combined and dried with anhydrous MgSO4, filtered and concentrated. The residue was purified by silica gel column chromatography using ethyl acetate/hexane (v/v=10/90) as eluent to obtain 2-methylbenzimidazole derivatives or methanol/dichloromethane (v/v=1/99) as eluent to obtain 5-iodo-2-methylbenzimidazole derivatives. The structures of the resulting benzimidazole derivatives were characterized by 1H NMR, 13C NMR, FTIR and GC-MS, with known compounds mainly confirmed by comparison with literature data and unknown compounds additionally provided with HRMS data.

References

[1] Tetrahedron, 2011, vol. 67, # 41, p. 8027 - 8033

5-IODO-2-METHYLBENZIMIDAZOLESupplier

Tianjin Yao Technology Development Co., Ltd.
Tel
022-18902014291 18902014291
Email
byswxsb01@163.com
Shanghai Topbiochem Technology Co., Ltd
Tel
021-58170097
Email
info@topbiochem.com
Shanghai potentpharm CO.,Ltd
Tel
13524892556
Email
sales-cn@potentpharm.com
AstaTech (Chengdu) Pharma. Co., Ltd.
Tel
15928766785 15928766785
Email
wupengcheng@astatech.cn
Shanghai Xingui Biotechnology Co., Ltd.
Tel
15121041756
Email
xingui2022@126.com