3-tert-Butylcyclobutanecarboxylic acid is an organic compound characterized by its cyclobutane ring structure, which is substituted with a tert-butyl group and a carboxylic acid functional group. This compound features a four-membered carbon ring, providing unique strain and reactivity compared to larger cyclic structures. The presence of the tert-butyl group enhances its steric bulk, influencing its physical and chemical properties, such as solubility and boiling point. The carboxylic acid group contributes to its acidity and potential for hydrogen bonding, which can affect its interactions in various chemical environments. Typically, compounds like this may exhibit moderate to low solubility in non-polar solvents and varying solubility in polar solvents, depending on the balance between hydrophobic and hydrophilic characteristics. Additionally, the compound may participate in typical carboxylic acid reactions, such as esterification and acid-base reactions. Its unique structure and functional groups make it of interest in organic synthesis and materials science, particularly in the development of novel compounds with specific properties.

3-tert-butylcyclobutanecarboxylic acid

66016-27-1: 3-tert-Butylcyclobutanecarboxylic acid is an organic compound characterized by its cyclobutane ring structure, which is substituted with a tert-butyl group and a carboxylic acid functional group. This compound features a four-membered carbon ring, providing unique strain and reactivity compared to larger cyclic structures. The presence of the tert-butyl group enhances its steric bulk, influencing its physical and chemical properties, such as solubility and boiling point. The carboxylic acid group contributes to its acidity and potential for hydrogen bonding, which can affect its interactions in various chemical environments. Typically, compounds like this may exhibit moderate to low solubility in non-polar solvents and varying solubility in polar solvents, depending on the balance between hydrophobic and hydrophilic characteristics. Additionally, the compound may participate in typical carboxylic acid reactions, such as esterification and acid-base reactions. Its unique structure and functional groups make it of interest in organic synthesis and materials science, particularly in the development of novel compounds with specific properties.

CAS 66016-27-1

3-tert-butylcyclobutanecarboxylic acid

3-tert-butylcyclobutane-1-carboxylic acid

Ref: IN-DA00FX84

3-tert-Butylcyclobutane-1-carboxylic acid

Ref: 3D-RCA01627