1,3-Cyclooctadiene is a cyclic diene with the molecular formula C8H12, characterized by its two double bonds located at the 1 and 3 positions of an eight-membered carbon ring. This compound is a colorless liquid at room temperature and possesses a distinctive odor. It is known for its reactivity, particularly in Diels-Alder reactions, making it valuable in organic synthesis and the production of various chemical intermediates. The presence of the double bonds contributes to its unsaturation, which influences its chemical behavior, including its ability to undergo polymerization. 1,3-Cyclooctadiene is also used as a ligand in coordination chemistry and can form complexes with transition metals. Its physical properties include a relatively low boiling point and moderate solubility in organic solvents. Safety considerations should be taken into account, as it may pose health risks upon exposure, necessitating proper handling and storage protocols in laboratory settings. Overall, 1,3-Cyclooctadiene is an important compound in both industrial and academic chemistry contexts.

1,3-Cyclooctadiene

1700-10-3: (Z,Z)-Cycloocta-1,3-diene, 1,3-Cyclooctadiene, Cycloocta-1,3-Diene, NSC 105773, NSC 72422, cis,cis-1,3-Cyclooctadiene

1,3-Cyclooctadiene (stabilized with TBC)

1,3-CYCLOOCTADIENE

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1,3-Cyclooctadiene, 97%

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CAS 1700-10-3: 1,3-Cyclooctadiene

1,3-Cyclooctadiene (stabilized with TBC)

Ref: 3B-C0502

1,3-CYCLOOCTADIENE

Ref: IN-DA003DIF

1,3-Cyclooctadiene, 97%

Ref: 02-L10516

1,3-Cyclooctadiene

Ref: 54-OR98232

1,3-Cyclooctadiene

Ref: 3D-BAA70010