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1,4-Cyclohexadiene is used to study the formation of parent ion from heavy fragmentation on irradiation with a high-intensity laser pulse. It is also used as a very effective hydrogen donor for catalytic hydrogenation reaction. It forms benzene at elevated temperatures in the presence of a ruthenium(II)-triphenylphosphine catalyst.
Mao, J. X.; Mathers, R. T. Damodaran, K. NMR spectroscopic and computational investigations of RuHCl(CO)(PPh3)3 catalyzed isomerization of 1,4-cyclohexadiene. J. Organomet. Chem. 2013, 741-742, 15-19.
Levandowski, B. J.; Houk, K. N. Theoretical Analysis of Reactivity Patterns in Diels-Alder Reactions of Cyclopentadiene, Cyclohexadiene, and Cycloheptadiene with Symmetrical and Unsymmetrical Dienophiles. J. Org. Chem. 2015, 80 (7), 3530-3537.
Kakinuma, S.; Shirota, H. Dynamic Kerr Effect Study on Six-Membered-Ring Molecular Liquids: Benzene, 1,3-Cyclohexadiene, 1,4-Cyclohexadiene, Cyclohexene, and Cyclohexane. J. Phys. Chem. B. 2015, 119 (13), 4713-4724.
Gefahrenhinweise (EU): H225-H340-H350-H304
Highly flammable liquid and vapour. May cause genetic defects. May cause cancer. May be fatal if swallowed and enters airways.
Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Obtain special instructions before use. IF SWALLOWED: IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.