1,3-Cyclooctanedione, with the CAS number 935-29-5, is a cyclic diketone characterized by its eight-membered carbon ring structure containing two carbonyl (C=O) groups located at the 1 and 3 positions. This compound is a colorless to pale yellow liquid at room temperature and has a distinctive odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. The presence of the diketone functional groups imparts reactivity, allowing it to participate in various chemical reactions, including condensation and oxidation. 1,3-Cyclooctanedione is of interest in organic synthesis and can serve as a building block for more complex molecules. Additionally, it exhibits potential applications in the fields of materials science and pharmaceuticals. Its stability and reactivity make it a valuable compound for research and industrial applications, although handling should be done with care due to potential health hazards associated with diketones.

1,3-Cyclooctanedione

935-29-5: 1,3-Cyclooctanedione, with the CAS number 935-29-5, is a cyclic diketone characterized by its eight-membered carbon ring structure containing two carbonyl (C=O) groups located at the 1 and 3 positions. This compound is a colorless to pale yellow liquid at room temperature and has a distinctive odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. The presence of the diketone functional groups imparts reactivity, allowing it to participate in various chemical reactions, including condensation and oxidation. 1,3-Cyclooctanedione is of interest in organic synthesis and can serve as a building block for more complex molecules. Additionally, it exhibits potential applications in the fields of materials science and pharmaceuticals. Its stability and reactivity make it a valuable compound for research and industrial applications, although handling should be done with care due to potential health hazards associated with diketones.

Cyclooctane-1,3-dione is a molecule with the molecular formula C8H12O4. It has a cyclic structure and is a bioorthogonal tag that can be used to create small molecules in living cells by photocycloaddition reactions. This synthetic molecule is an azide that reacts with benzene to form cyclobutane rings. Cyclooctane-1,3-dione can be used in large-scale production methods such as those employed for making polymers such as polyethylene terephthalate (PET).

CAS 935-29-5

1,3-Cyclooctanedione

Cyclooctane-1,3-dione

Ref: 3D-AAA93529