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  2. 1-Ethynylcyclohexanol - Wikipedia

    en.wikipedia.org/wiki/1-Ethynylcyclohexanol

    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]

  3. Cyclohexane-1,2,3,4,5,6-hexol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane-1,2,3,4,5,6-hexol

    The crystal structure is monoclinic with the / group. The crystal cell parameters are a = 1014.35 pm , b = 815.42 pm, c = 862.39 pm, β = 92.3556 ° , Z = 4. The cell volume is 0.71270 nm 3 , or about 0.178 nm 3 per molecule (which is a bit smaller than the typical volumes of other isomers).

  4. Ethinamate - Wikipedia

    en.wikipedia.org/wiki/Ethinamate

    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 ...

  5. CAS Registry Number - Wikipedia

    en.wikipedia.org/wiki/CAS_Registry_Number

    Screenshot of the CAS Common Chemistry database with information about caffeine ().. A CAS Registry Number [1] (also referred to as CAS RN [2] or informally CAS Number) is a unique identification number, assigned by the Chemical Abstracts Service (CAS) in the US to every chemical substance described in the open scientific literature, in order to index the substance in the CAS Registry.

  6. Ethynyl group - Wikipedia

    en.wikipedia.org/wiki/Ethynyl_group

    In organic chemistry, an ethynyl group is a functional group with the formula −C≡CH. It is the acetylene molecule with one fewer hydrogen atom.. Ethynyl group (HC≡C–), also designated as acetylenic group (from acetylene), and referred to in IUPAC chemical nomenclature as -yne suffix.

  7. Cyclohexanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanol

    Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [5]. 2 C 6 H 12 + O 2 → 2 C 6 H 11 OH. This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid.

  8. Xylene - Wikipedia

    en.wikipedia.org/wiki/Xylene

    The physical properties of the isomers of xylene differ slightly. 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).

  9. 1-Hexanol - Wikipedia

    en.wikipedia.org/wiki/1-Hexanol

    1-Hexanol (IUPAC name hexan-1-ol) is an organic alcohol with a six-carbon chain and a condensed structural formula of CH 3 (CH 2) 5 OH. This colorless liquid is slightly soluble in water, but miscible with diethyl ether and ethanol .

  1. Related searches 1 ethynylcyclohexanol cas no of base structure definition chart template

    1 etynyl cyclohexanolethylene cyclohexanol