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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. List of CAS numbers by chemical compound - Wikipedia

    en.wikipedia.org/wiki/List_of_CAS_numbers_by...

    Chemical formula Synonyms CAS number C 10 H 16 N 2 O 8: Ethylenediaminetetraacetic acid (EDTA): 6381–92–6 C 12 H 22 O 11: sucrose: 57–50–1 C 18 H 29 O 3 S: sodium dodecyl benzenesulfonate: 2155–30–0

  4. Sodium amide - Wikipedia

    en.wikipedia.org/wiki/Sodium_amide

    Usually two equivalents of sodium amide yields the desired alkyne. Three equivalents are necessary in the preparation of a terminal alkynes because the terminal CH of the resulting alkyne protonates an equivalent amount of base. Hydrogen chloride and ethanol can also be eliminated in this way, [11] as in the preparation of 1-ethoxy-1-butyne. [12]

  5. Acetic anhydride - Wikipedia

    en.wikipedia.org/wiki/Acetic_anhydride

    Acetic anhydride, or ethanoic anhydride, is the chemical compound with the formula (CH 3 CO) 2 O.Commonly abbreviated Ac 2 O, it is the simplest isolable anhydride of a carboxylic acid and is widely used as a reagent in organic synthesis.

  6. 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.

  7. Dimethylacetamide - Wikipedia

    en.wikipedia.org/wiki/Dimethylacetamide

    The chemical reactions of dimethylacetamide are typical of N,N-disubstituted amides. Hydrolysis of the acyl-N bond occurs in the presence of acids: . CH 3 CON(CH 3) 2 + H 2 O + HCl → CH 3 COOH + (CH 3) 2 NH 2 + Cl −

  8. Cyclohexane (data page) - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_(data_page)

    Liquid properties Std enthalpy change of formation, Δ f H o liquid –156.4 kJ/mol Standard molar entropy, S o liquid: 204 J/(mol K) Enthalpy of combustion, Δ c H o –3919.6 kJ/mol Heat capacity, c p: 156 J/(mol K) or 1.85 J/(g K) Gas properties Std enthalpy change of formation, Δ f H o gas –123.1 kJ/mol Standard molar entropy, S o gas ...

  9. Propargyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Propargyl_alcohol

    Propargyl alcohol, or 2-propyn-1-ol, is an organic compound with the formula C 3 H 4 O. It is the simplest stable alcohol containing an alkyne functional group. [ 3 ] Propargyl alcohol is a colorless viscous liquid that is miscible with water and most polar organic solvents.

  1. Related searches 1 ethynylcyclohexanol cas no of base structure solution chemistry liquid

    1 etynyl cyclohexanolethylene cyclohexanol