N-(1-Cyclohexen-1-yl)morpholine manufacturers
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| | N-(1-Cyclohexen-1-yl)morpholine Basic information |
| | N-(1-Cyclohexen-1-yl)morpholine Chemical Properties |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37/39 | | WGK Germany | 3 | | F | 9 | | TSCA | TSCA listed | | HS Code | 29349990 | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | N-(1-Cyclohexen-1-yl)morpholine Usage And Synthesis |
| Description |
1-Morpholinocyclohexene (N-(1-Cyclohexen-1-yl)morpholine) falls under the category of organic compounds called morpholine class of heterocyclic amines. This colorless liquid possesses a distinct amine-like odor and displays remarkable versatility with widespread applications in multiple industries, including agrochemicals and cosmetics. Moreover, it is a valuable solvent, corrosion inhibitor, and integral component in lubricants[1].
| | Chemical Properties | CLEAR COLOURLESS TO LIGHT YELLOW LIQUID | | Synthesis Reference(s) | Synthesis, p. 529, 1984 DOI: 10.1055/s-1984-30893 | | Synthesis | The general procedure for the synthesis of 1-morpholino-1-cyclohexene from morpholine and cyclohexanone is as follows: to a solution of morpholine (10.5 mL, 0.12 mol, 1.2 eq.) in anhydrous toluene (70 mL) was added cyclohexanone (10.4 mL, 0.10 mol, 1.0 eq.), followed by the addition of p-toluenesulfonic acid (0.20 g, 1.16 mmol. 0.016 eq.) as a catalyst. The reaction mixture was heated to reflux for 5 hours. Upon completion of the reaction, the reaction solution was cooled and subsequently concentrated under reduced pressure to afford the target product 1-morpholino-1-cyclohexene in 85% yield. | | References | [1] R. Nesi. “Reactions of 3,5-dimethyl-4-nitroisoxazole with cyclic enamines and 1-diethylaminopropyne.” Heterocycles 32 1 (1991): 1913–1921.
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| | N-(1-Cyclohexen-1-yl)morpholine Preparation Products And Raw materials |
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