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1-Ethynylcyclohexanol (ECX) is an alkynyl alcohol derivative which is both a synthetic precursor to, and an active metabolite of the tranquilizer ethinamate, and has similar sedative, anticonvulsant and muscle relaxant effects. It has been sold as a designer drug, first being identified in the UK in March 2012. [1] [2] [3] [4]
Ethinamate (1-ethynylcyclohexanone carbamate) is synthesized by combining acetylene with cyclohexanone to make 1-ethynylcyclohexanol, and then transforming this into a carbamate by the subsequent reaction with phosgene, and later with ammonia. Some lithium metal or similar is used to make the acetylene react with the cyclohexanone in the first ...
N 2: nitrogen: 7727-37-9 [1] N 2 F 2: dinitrogen difluoride: 13812–43–6 N 2 F 4: dinitrogen tetrafluoride: 10036–47–2 N 2 O: dinitrogen monoxide: 10024–97–2 N 2 O 3: dinitrogen trioxide: 10544–73–7 N 2 O 4: dinitrogen tetroxide: 10544–72–6 N 2 O 5: dinitrogen pentoxide: 10102–03–1 NaAlCl 4: sodium tetracholoraluminate ...
Ethylene glycol (IUPAC name: ethane-1,2-diol) is an organic compound (a vicinal diol [7]) with the formula (CH 2 OH) 2.It is mainly used for two purposes: as a raw material in the manufacture of polyester fibers and for antifreeze formulations.
The melting point ranges from −47.87 °C (−54.17 °F) (m-xylene) to 13.26 °C (55.87 °F) (p-xylene)—as usual, the para isomer's melting point is much higher because it packs more readily in the crystal structure. The boiling point for each isomer is around 140 °C (284 °F).
E)-Stilbene, commonly known as trans-stilbene, is an organic compound represented by the condensed structural formula C 6 H 5 CH=CHC 6 H 5. Classified as a diarylethene , it features a central ethylene moiety with one phenyl group substituent on each end of the carbon–carbon double bond .
In organic chemistry, an ethynyl group is a functional group with the formula −C≡CH, representing an acetylene molecule with one fewer hydrogen atom.. Ethynyl group (HC≡C–), also designated as an acetylenic group (from acetylene), is referred to in IUPAC chemical nomenclature with the -yne suffix.
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