2-Methyl-2-(4-nitrophenyl)propanoic acid, with the CAS number 42206-47-3, is an organic compound characterized by its carboxylic acid functional group and a nitrophenyl substituent. This compound features a branched alkyl chain, specifically a 2-methyl group, which contributes to its steric properties. The presence of the nitro group (–NO2) on the para position of the phenyl ring enhances its electron-withdrawing characteristics, influencing its reactivity and solubility in various solvents. Typically, compounds like this exhibit moderate to high polarity due to the carboxylic acid group, which can engage in hydrogen bonding. The molecular structure suggests potential applications in organic synthesis, pharmaceuticals, or as intermediates in chemical reactions. Additionally, the compound's stability and reactivity can be affected by factors such as pH and temperature, making it important to consider these conditions in practical applications. Overall, 2-methyl-2-(4-nitrophenyl)propanoic acid is a notable compound in organic chemistry with specific functional properties that can be utilized in various chemical contexts.

2-methyl-2-(4-nitrophenyl)propanoic acid

42206-47-3: Benzeneacetic acid, alpha,alpha-dimethyl-4-nitro-, 2-Methyl-2-(4-nitrophenyl)propanoic acid

CAS 42206-47-3: 2-methyl-2-(4-nitrophenyl)propanoic acid

2-methyl-2-(4-nitrophenyl)propanoic acid

Ref: IN-DA00BZPX

2-Methyl-2-(4-nitrophenyl)propanoic acid

Ref: 3D-SBA20647

2-Methyl-2-(4-nitrophenyl)propanoic acid

Ref: 54-OR16879

2-Methyl-2-(4-nitrophenyl)-propionic acid

Ref: 10-F040587