Benzenebutanoic acid, α-hydroxy-α-methyl- (CAS 4374-63-4) is an organic compound characterized by its aromatic and aliphatic functional groups. It features a benzenoid ring attached to a butanoic acid chain, with a hydroxyl group and a methyl group positioned at the alpha carbon relative to the carboxylic acid. This structure imparts both hydrophilic and hydrophobic properties, making it soluble in organic solvents while exhibiting some solubility in water due to the presence of the hydroxyl group. The compound is likely to participate in various chemical reactions typical of carboxylic acids, such as esterification and acid-base reactions. Its unique structure may also influence its biological activity, potentially making it relevant in pharmaceutical applications or as an intermediate in organic synthesis. The compound's stability, reactivity, and potential applications can be further explored through its interactions with other chemical species and its behavior under different environmental conditions.

Benzenebutanoic acid, a-hydroxy-a-methyl-

4374-63-4: Benzenebutanoic acid, α-hydroxy-α-methyl- (CAS 4374-63-4) is an organic compound characterized by its aromatic and aliphatic functional groups. It features a benzenoid ring attached to a butanoic acid chain, with a hydroxyl group and a methyl group positioned at the alpha carbon relative to the carboxylic acid. This structure imparts both hydrophilic and hydrophobic properties, making it soluble in organic solvents while exhibiting some solubility in water due to the presence of the hydroxyl group. The compound is likely to participate in various chemical reactions typical of carboxylic acids, such as esterification and acid-base reactions. Its unique structure may also influence its biological activity, potentially making it relevant in pharmaceutical applications or as an intermediate in organic synthesis. The compound's stability, reactivity, and potential applications can be further explored through its interactions with other chemical species and its behavior under different environmental conditions.

<p>Naproxen is a nonsteroidal anti-inflammatory drug (NSAID) that is used to treat pain and inflammation. It inhibits the enzyme cyclooxygenase, which is required for the production of prostaglandins. Naproxen has high enantioselectivity when reacting with nitriles and dinitriles because it acts as a diacid or amid acid in these reactions. This means that naproxen preferentially reacts with the 2-hydroxy group of an acyl chloride or ester, forming an amide or amidine respectively. It also has an ability to inhibit bacterial strains such as those from Streptococcus pyogenes and Staphylococcus aureus. Naproxen may act by substituting for the carboxylic acid groups of the bacterial cell wall, where it can form a covalent bond with glutamic acid residues on the cell wall surface.</p>

CAS 4374-63-4

Benzenebutanoic acid, a-hydroxy-a-methyl-

2-Hydroxy-2-methyl-4-phenylbutanoic acid

Ref: 3D-EAA37463