Cyclohexene, 99% stab.

General References:

1. Protection of the phenolic OH of tyrosine as the cyclohexyl ether has been effected with BF₃ etherate. The group can be cleaved with HF or HBr/AcOH: J. Am. Chem. Soc., 100, 3559 (1978).
2. Hydrogen donor in catalytic hydrogen-transfer reactions, usually with palladium. For reviews, see: Chem. Rev., 74, 567 (1974); 85, 129 (1985). Examples:
3. Hydrogenolysis of benzyloxycarbonyl groups: Synthesis, 685 (1976). Simultaneous cleavage of benzyl and benzyloxycarbonyl groups: J. Chem. Soc., Perkin 1, 490 (1977). Cleavage of benzyl ethers: Synthesis, 396 (1981). With FeCl₃, reduction of aryl carbonyl groups to methylene: J. Chem. Soc., Chem. Commun., 757 (1976).
4. Conditions have been described for work-up of the ozonide to give the monoacetal of the dialdehyde, the aldehydo-ester, or the dimethyl acetal of the methyl ester: Org. Synth. Coll., 7, 168 (1990).
5. Undergoes allylic acetoxylation, catalyzed by Palladium(II) acetate, 10516 , in the presence of MnO₂ and 1,4-benzoquinone: Org. Synth. Coll., 8, 137 (1993).
6. Xu, L. Q.; Chen, J. C.; Qian, S. S.; Zhang, A. K.; Fu, G. D.; Li, C. M.; Kang, E. T. PEGylated Metalloporphyrin Nanoparticles as a Promising Catalyst for the Heterogeneous Oxidation of Cyclohexene in Water. Macromol. Chem. Phys. 2015, 216 (4), 417-426.
7. Hu, X.; Shi, Y.; Zhang, Y.; Zhu, B.; Zhang, S.; Huang, W. Nanotubular TiO₂-supported amorphous Co-B catalysts and their catalytic performances for hydroformylation of cyclohexene. Catal. Commun. 2015, 59, 45-49.