CDDA, or 1,3-Cyclohexanedione, is a chemical compound characterized by its diketone structure, which features two carbonyl groups (C=O) within a six-membered cyclohexane ring. This compound is typically a colorless to pale yellow liquid or solid, depending on its specific form and purity. CDDA is known for its reactivity, particularly in condensation reactions, where it can form various derivatives and complexes. It is soluble in organic solvents such as ethanol and acetone but has limited solubility in water. The compound is utilized in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and as an intermediate in various chemical reactions. Additionally, CDDA exhibits interesting properties such as the ability to participate in Michael additions and other nucleophilic reactions, making it valuable in synthetic organic chemistry. Safety data indicates that, like many diketones, it should be handled with care, as it may pose health risks upon exposure.

CDDA

41892-01-7: CDDA, or 1,3-Cyclohexanedione, is a chemical compound characterized by its diketone structure, which features two carbonyl groups (C=O) within a six-membered cyclohexane ring. This compound is typically a colorless to pale yellow liquid or solid, depending on its specific form and purity. CDDA is known for its reactivity, particularly in condensation reactions, where it can form various derivatives and complexes. It is soluble in organic solvents such as ethanol and acetone but has limited solubility in water. The compound is utilized in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and as an intermediate in various chemical reactions. Additionally, CDDA exhibits interesting properties such as the ability to participate in Michael additions and other nucleophilic reactions, making it valuable in synthetic organic chemistry. Safety data indicates that, like many diketones, it should be handled with care, as it may pose health risks upon exposure.

CAS 41892-01-7

CDDA