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Thermo Scientific Chemicals
Cyclohexylacetylene, 98%
CAS: 931-48-6 | C8H12 | 108.184 g/mol
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CAS931-48-6
IUPAC Nameethynylcyclohexane
Molecular FormulaC8H12
InChI KeySSDZYLQUYMOSAK-UHFFFAOYSA-N
SMILESC#CC1CCCCC1
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規格表Cyclohexylacetylene is used in the preparation of hydrido-vinylidene complexes of osmium, which finds vital intermediates in several homogeneous and heterogeneous catalytic reactions such as alkene olimerization, polymerization and Fischer-Tropsch synthesis.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Cyclohexylacetylene is used in the preparation of hydrido-vinylidene complexes of osmium, which finds vital intermediates in several homogeneous and heterogeneous catalytic reactions such as alkene olimerization, polymerization and Fischer-Tropsch synthesis.
Solubility
Immiscible with water.
Notes
Incompatible with strong oxidizing agents.
Cyclohexylacetylene is used in the preparation of hydrido-vinylidene complexes of osmium, which finds vital intermediates in several homogeneous and heterogeneous catalytic reactions such as alkene olimerization, polymerization and Fischer-Tropsch synthesis.
Solubility
Immiscible with water.
Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Jacquet, J.; Auvinet, A. L.; Mandadapu, A. K.; Haddad, M.; Ratovelomanana-Vidal, V.; Michelet, V. Practical Solvent-Free Ruthenium Trichloride-Mediated Benzannulation Approach to Fused Functionalized Arenes. Adv. Synth. Catal. 2015, 357 (7), 1387-1392.
- Zhang, A. L.; Yang, L. W.; Yang, N. F.; Zhang, J. Synthesis of enantiopure C3-symmetric bulky trialkanolamines and their enantioselective inductivity during the alkynylation of aldehydes. J. Organomet. Chem. 2015, 775, 88-93.