3-Bromo-N-(2-hydroxy-1,1-dimethylethyl)-2-methylbenzamide, identified by its CAS number 1331185-69-3, is an organic compound characterized by its bromine substitution and amide functional group. This compound features a benzene ring with a methyl group and a bromine atom at specific positions, along with a side chain that includes a hydroxyl group and a tert-butyl group. The presence of the hydroxyl group contributes to its potential solubility in polar solvents, while the bulky tert-butyl group may influence its steric properties and reactivity. The compound's structure suggests it may exhibit interesting biological activities, making it a candidate for pharmaceutical research. Its synthesis and characterization would typically involve standard organic chemistry techniques, including NMR and mass spectrometry for confirmation of structure. As with many brominated compounds, it is essential to consider its environmental impact and potential toxicity, particularly in biological systems. Overall, this compound represents a unique combination of functional groups that may lead to diverse applications in medicinal chemistry and material science.

3-BroMo-N-(2-hydroxy-1,1-diMethylethyl)-2-Methyl-benzaMide

1331185-69-3: 3-Bromo-N-(2-hydroxy-1,1-dimethylethyl)-2-methylbenzamide, identified by its CAS number 1331185-69-3, is an organic compound characterized by its bromine substitution and amide functional group. This compound features a benzene ring with a methyl group and a bromine atom at specific positions, along with a side chain that includes a hydroxyl group and a tert-butyl group. The presence of the hydroxyl group contributes to its potential solubility in polar solvents, while the bulky tert-butyl group may influence its steric properties and reactivity. The compound's structure suggests it may exhibit interesting biological activities, making it a candidate for pharmaceutical research. Its synthesis and characterization would typically involve standard organic chemistry techniques, including NMR and mass spectrometry for confirmation of structure. As with many brominated compounds, it is essential to consider its environmental impact and potential toxicity, particularly in biological systems. Overall, this compound represents a unique combination of functional groups that may lead to diverse applications in medicinal chemistry and material science.

<p>Applications 3-Bromo-N-(2-hydroxy-1,1-dimethylethyl)-2-methyl-benzamide is a reactant used in the preparation of hydroxymethylphenylethylimidazolethione derivatives for use in treatment of chronic pain.<br></p>

CAS 1331185-69-3

3-BroMo-N-(2-hydroxy-1,1-diMethylethyl)-2-Methyl-benzaMide

3-Bromo-N-(2-hydroxy-1,1-dimethylethyl)-2-methyl-benzamide

Ref: TR-B684595