5-Bromo-1,3-dihydrobenzoimidazol-2-one

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Products Intro: Product Name:ethyl 1,3-oxazole-4-carboxylate
CAS:39513-26-3
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G
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Products Intro: Product Name:5-Bromo-1,3-dihydrobenzoimidazol-2-one
CAS:39513-26-3
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Products Intro: Product Name:5-Bromo-1,3-dihydrobenzoimidazol-2-one
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CAS:39513-26-3
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Products Intro: Product Name:5-Bromo-1,3-dihydrobenzoimidazol-2-one
CAS:39513-26-3
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5-Bromo-1,3-dihydrobenzoimidazol-2-one manufacturers

5-Bromo-1,3-dihydrobenzoimidazol-2-one Basic information
Product Name:5-Bromo-1,3-dihydrobenzoimidazol-2-one
Synonyms:5-BROMO-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE;5-BROMO-1,3-DIHYDRO-BENZOIMIDAZOL-2-ONE;5-BROMO-1H-BENZO[D]IMIDAZOL-2(3H)-ONE;5-Bromobenzo[d]imidazol-2-one;5-Bromo-1,3-dihyrobenzoimidazol-2-one;5-BROMO-1,3-DIHYDROBENZOIMIDAZOL-2-ONE, 95+%;5-Bromo-1,3-dihydro-2H-benzimidazol-2-one;5-Bromo-2,3-dihydro-2-oxo-1H-benzimidazole
CAS:39513-26-3
MF:C7H5BrN2O
MW:213.03
EINECS:
Product Categories:
Mol File:39513-26-3.mol
5-Bromo-1,3-dihydrobenzoimidazol-2-one Structure
5-Bromo-1,3-dihydrobenzoimidazol-2-one Chemical Properties
Melting point 336-337 °C(Solv: acetic acid (64-19-7))
Boiling point 180.0±19.0 °C(Predicted)
density 1.728±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka11.18±0.30(Predicted)
AppearanceLight brown to gray Solid
InChIInChI=1S/C7H5BrN2O/c8-4-1-2-5-6(3-4)10-7(11)9-5/h1-3H,(H2,9,10,11)
InChIKeyVWIGEYVTDXNDHV-UHFFFAOYSA-N
SMILESC1(=O)NC2=CC=C(Br)C=C2N1
Safety Information
Hazard Codes Xn
Risk Statements 22
HS Code 2933998090
MSDS Information
5-Bromo-1,3-dihydrobenzoimidazol-2-one Usage And Synthesis
Synthesis
1,1'-Carbonyldiimidazole

530-62-1

4-Bromo-1,2-benzenediamine

1575-37-7

5-Bromo-1,3-dihydrobenzoimidazol-2-one

39513-26-3

2.1A. General procedure for the synthesis of 5-bromo-1,3-dihydrobenzimidazol-2-one: 4.29 g (26.46 mmol) of N,N'-carbonyldiimidazole (CDI) was added to 95 mL of N,N-dimethylformamide (DMF) solution containing 4.5 g (24.05 mmol) of 4-bromobenzene-1,2-diamine. The reaction mixture was stirred at 80 °C for 5 hours. After completion of the reaction, the mixture was poured into water and the precipitate formed was filtered out. The precipitate was washed three times with water and subsequently dried in a circulating air dryer at 60 °C. Yield: 4.6 g (90% of theoretical yield); Molecular formula: C7H5BrN2O (M = 213.03); Calculated value: molecular ion peak (M + H)+: 213/215; Measured value: molecular ion peak (M + H)+: 213/215; Rf-value: 0.5 (silica gel, dichloromethane/methanol = 10:1).

References[1] Journal of Medicinal Chemistry, 2016, vol. 59, # 15, p. 7188 - 7211
[2] Patent: US2005/267115, 2005, A1. Location in patent: Page/Page column 35
[3] Patent: WO2005/103029, 2005, A1. Location in patent: Page/Page column 75
[4] Journal of Medicinal Chemistry, 2006, vol. 49, # 12, p. 3719 - 3742
[5] Patent: WO2011/130628, 2011, A1. Location in patent: Page/Page column 231
5-Bromo-1,3-dihydrobenzoimidazol-2-one Preparation Products And Raw materials
Raw materialsUrea-->1,1'-Carbonyldiimidazole-->Phenyl chloroformate-->4-Bromo-1,2-benzenediamine
Tag:5-Bromo-1,3-dihydrobenzoimidazol-2-one(39513-26-3) Related Product Information
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