| Weight | 124.183 g/mol |
|---|---|
| Formula | C8H12O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1-Ethynyl-1-cyclohexanol (78-27-3, 28652-54-2)
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- An unprecedented ruthenium allenylidene complex containing an unsaturated bicyclic system : formal addition of 1-ethynyl-1-cyclohexanol to an alkenylvinylidene intermediate complex (Organometallics, 1994)
- Polymerization of 1-Ethynyl-1-Cyclohexanol by Transition Metal Catalysts (Journal of Macromolecular Science, Part A, 1994)
- Polymerlzatlon of 1-Ethynyl-1-Cyclohexanol by Radiation, Electroinitiation, and Chemical Catalysts (Journal of Macromolecular Science, Part A, 1992)
- Using 1-ethynyl-2,2,6-trimethyl-cyclohexanol to enhance woody fragrance of perfume compositions (1980)
- Verwendung von 1-aethynyl-2,2,6- trimethyl-cyclohexanol als parfuem- und aromabestandteil Use of 1-ethynyl-2,2,6- trimethyl-cyclohexanol as perfume and flavor constituents (1980)
- Unusual activation of 1-ethynyl-1-cyclohexanol by [RuCl(5-C9H7)(PPh3)2]: synthesis and reactivity of the allenylidene derivative [Ru{CCC(C13H20)}(5-C9H7)(PPh3)2][PF6] (Journal of The Chemical Society-dalton Transactions, 1999)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC#CC1(CCCCC1)O
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InChIKeyQYLFHLNFIHBCPR-UHFFFAOYSA-N
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