6-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-benzimidazole
- Product Name
- 6-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-benzimidazole
- CAS No.
- 1245649-58-4
- Chemical Name
- 6-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-benzimidazole
- Synonyms
- 6-bromo-1-(oxan-4-yl)benzimidazole;6-Bromo-1-(tetrahydro-2H-pyran-4-yl);6-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-benzimidazole;1H-Benzimidazole, 6-bromo-1-(tetrahydro-2H-pyran-4-yl)-
- CBNumber
- CB32534674
- Molecular Formula
- C12H13BrN2O
- Formula Weight
- 281.15
- MOL File
- 1245649-58-4.mol
6-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-benzimidazole Property
- Boiling point:
- 425.3±55.0 °C(Predicted)
- Density
- 1.60
- storage temp.
- Inert atmosphere,Room Temperature
- pka
- 4.10±0.10(Predicted)
N-Bromosuccinimide Price
- Product number
- 4647AA
- Product name
- 6-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-benzo[d]imidazole
- Packaging
- 100mg
- Price
- $84
- Updated
- 2021/12/16
- Product number
- HCH0367685
- Product name
- 6-BROMO-1-(TETRAHYDRO-2H-PYRAN-4-YL)-1H-BENZO[D]IMIDAZOLE
- Purity
- 95.00%
- Packaging
- 250MG
- Price
- $347.55
- Updated
- 2021/12/16
- Product number
- 093302
- Product name
- 6-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-benzo[d]imidazole
- Purity
- 95+%
- Packaging
- 250mg
- Price
- $378
- Updated
- 2021/12/16
- Product number
- 093302
- Product name
- 6-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-benzo[d]imidazole
- Purity
- 95+%
- Packaging
- 1g
- Price
- $807
- Updated
- 2021/12/16
- Product number
- A116653
- Product name
- 6-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-benzo[d]imidazole
- Purity
- 98%
- Packaging
- 100mg
- Price
- $21
- Updated
- 2021/12/16
6-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-benzimidazole Chemical Properties,Usage,Production
Synthesis
1162697-10-0
149-73-5
1245649-58-4
GENERAL STEPS: To a solution of trimethyl orthoformate (2 mL) of 5-bromo-N1-(tetrahydro-2H-pyran-4-yl)benzene-1,2-diamine (500 mg, 1.852 mmol) was added p-toluenesulfonic acid (TsOH, 15 mg, 0.0789 mmol). The reaction mixture was stirred at 100 °C for 12 hours. After completion of the reaction, the reaction mixture was extracted with dichloromethane (DCM), the organic layer was washed with water and then dried with anhydrous sodium sulfate. After filtration to remove the desiccant, the filtrate was concentrated and purified by column chromatography to give the crude product (201 mg, 38.53% yield).LCMS (m/z): 281.0, 283.0 ([M + H]+).
References
[1] Patent: WO2014/100695, 2014, A1. Location in patent: Paragraph 00344
6-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-benzimidazole Preparation Products And Raw materials
Raw materials
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