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5-Bromo-6-methoxybenzoimidazole

Product Name
5-Bromo-6-methoxybenzoimidazole
CAS No.
1008361-65-6
Chemical Name
5-Bromo-6-methoxybenzoimidazole
Synonyms
5-Bromo-6-methoxybenzimidazole;5-Bromo-6-methoxybenzoimidazole;6-Bromo-5-methoxy-1H-benzimidazole;5-Bromo-6-methoxybenzimidazole 97%;1H-Benzimidazole, 6-bromo-5-methoxy-;5-bromo-6-methoxy-1H-1,3-benzodiazole;5-Bromo-6-methoxy-1H-benzo[d]imidazole
CBNumber
CB02522333
Molecular Formula
C8H7BrN2O
Formula Weight
227.06
MOL File
1008361-65-6.mol
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5-Bromo-6-methoxybenzoimidazole Property

Boiling point:
435.7±25.0 °C(Predicted)
Density 
1.678±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
12.43±0.30(Predicted)
Appearance
White to yellow Solid
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Safety

HS Code 
2933299090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
B696598
Product name
5-Bromo-6-methoxybenzoimidazole
Packaging
25mg
Price
$45
Updated
2021/12/16
TRC
Product number
B696598
Product name
5-Bromo-6-methoxybenzoimidazole
Packaging
250mg
Price
$125
Updated
2021/12/16
AK Scientific
Product number
Z3795
Product name
5-Bromo-6-methoxy-1H-benzo[d]imidazole
Packaging
250mg
Price
$130
Updated
2021/12/16
Apolloscientific
Product number
OR400542
Product name
5-Bromo-6-methoxybenzimidazole
Purity
97%
Packaging
250mg
Price
$135
Updated
2021/12/16
SynQuest Laboratories
Product number
4H56-9-4K
Product name
5-Bromo-6-methoxybenzimidazole
Packaging
250mg
Price
$160
Updated
2021/12/16
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5-Bromo-6-methoxybenzoimidazole Chemical Properties,Usage,Production

Synthesis

64-18-6

108447-01-4

1008361-65-6

Step 2: Formic acid (1 mL) was added to a mixed solution of 4-bromo-5-methoxybenzene-1,2-diamine (3.8 g, 18 mmol) and triethyl orthoformate (50 mL) prepared in Step 1 under stirring conditions. The reaction mixture was heated to reflux for 3 hours and subsequently concentrated under reduced pressure. The concentrated residue was extracted by partitioning with ethyl acetate (200 mL) and 1N aqueous sodium carbonate solution (100 mL). The organic layer (ethyl acetate layer) was separated, washed with brine (100 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 5-bromo-6-methoxy-1H-benzo[d]imidazole (4.0 g) as a brown oil. The product was used directly in the subsequent reaction without further purification.LCMS (ESI) m/z 228 and 230 (M + H)+.

References

[1] Patent: EP2766359, 2016, B1. Location in patent: Paragraph 0472

5-Bromo-6-methoxybenzoimidazole Preparation Products And Raw materials

Raw materials

Preparation Products

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