2-(6-(2,5-dichloropyrimidin-4-yl)-4-fluoro-1-isopropyl-1H-benzo[d]imidazol-2-yl)propan-2-ol

2-(6-(2,5-dichloropyrimidin-4-yl)-4-fluoro-1-isopropyl-1H-benzo[d]imidazol-2-yl)propan-2-ol

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4-bromo-1-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one

$995.00
CAS No.: 1240593-33-2
Catalog No.: 197712
Purity: 95%
MF: C8H7BrN2O
MW: 227.061
Storage: 2-8 degree Celsius
SMILES: BrC1=CC=CC=2N(C(NC21)=O)C
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197712
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4-bromo-1-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one; CAS No.: 1240593-33-2;4-bromo-1-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one. PROPERTIES: 4-bromo-1-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one is a brominated heterocycle with a molecular weight of 234.06 g/mol. This white crystalline solid has a melting point between 175-178 C. The molecule features a benzo[d]imidazole ring system with dihydro substitution at positions 1 and 3, a bromo substituent at position 4, and a methyl group at position 1, bearing a ketone group at position 2. It demonstrates limited solubility in common organic solvents such as ethyl acetate and methanol but is sparingly soluble in water. Proper storage involves keeping in tightly sealed containers at room temperature, protected from light and moisture. Safety considerations include the bromine substituent's potential to cause skin irritation and the ketone group's moderate toxicity. Proper protective equipment should be utilized during handling. APPLICATIONS: This compound primarily serves as a building block in the synthesis of agrochemicals and pharmaceuticals, where the brominated imidazolone structure provides essential binding affinity to target enzymes. In medicinal chemistry, it has been employed in developing antimicrobial agents targeting bacterial and fungal pathogens and has shown utility in creating herbicides with selective activity against grassy weeds. The imidazolone scaffold has also been explored in materials science for developing fluorescent probes, leveraging the electron-deficient imidazole core to tune optical properties. These applications are documented in publications from the Journal of Medicinal Chemistry and the Journal of Fluorescence.

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