Cyclooctane-1,5-dione is a cyclic diketone characterized by its eight-membered carbon ring structure with two carbonyl (C=O) groups located at the 1 and 5 positions. This compound typically appears as a colorless to pale yellow liquid and is known for its distinctive odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. Cyclooctane-1,5-dione exhibits reactivity typical of diketones, including the ability to undergo condensation reactions and participate in various organic synthesis processes. Its molecular structure allows for potential applications in the synthesis of more complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the compound's unique ring strain and electronic properties can influence its reactivity and stability under different conditions. Safety precautions should be observed when handling this substance, as it may pose health risks if inhaled or ingested.

cyclooctane-1,5-dione

Cyclooctane-1,5-dione

Cyclooctane-1,5-dione is a cyclization reaction product of acetylation and conformation. It has been shown to have the same skeleton as ethanol and can be used as an analogue for ethanol in chemical reactions. Cyclooctane-1,5-dione is also soluble in ethanol solution and exhibits a five-membered cyclic structure. Cyclooctane-1,5-dione has been shown to react with diamines synchronously under acidic conditions to produce yields of aminocyclohexadienes. The compound has been found to crystallize in a monoclinic form at room temperature.

CAS 1489-74-3: cyclooctane-1,5-dione

Cyclooctane-1,5-dione

Ref: 54-OR26280

Cyclooctane-1,5-dione

Ref: 3D-BAA48974

1,5-Cyclooctanedione

Ref: IN-DA001LAB