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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]
This is a list of CAS numbers by chemical formulas and chemical compounds, indexed by formula.The CAS number is a unique number applied to a specific chemical by the Chemical Abstracts Service (CAS).This list complements alternative listings to be found at list of inorganic compounds and glossary of chemical formulae
Ortho esters are readily hydrolyzed in mild aqueous acid to form esters: . RC(OR ′) 3 + H 2 O → RCO 2 R ′ + 2 R ′ OH. For example, trimethyl orthoformate CH(OCH 3) 3 may be hydrolyzed (under acidic conditions) to methyl formate and methanol; [5] and may be further hydrolyzed (under alkaline conditions) to salts of formic acid and methanol.
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 ...
The carbon–oxygen bond length in these cations is near 1.1 Å (110-112 pm), which is shorter than the 112.8 pm of carbon monoxide and indicates triple-bond character. [ 5 ] [ 6 ] [ 7 ] The carbon centres of acylium ions generally have a linear geometry and sp atomic hybridization , and are best represented by a resonance structure bearing a ...
As early as 1938, G. N. Lewis pointed out that the relative strength of an acid or base depended upon the base or acid against which it was measured. [1] No single rank order of acid or base strength can predict the energetics of the cross reaction. Consider the following pair of acid–base reactions:. 4F-C 6 H 4 OH + OEt 2 −ΔH = 5.94 kcal/mole
Isethionic acid is an organosulfur compound containing an alkyl sulfonic acid located beta to a hydroxy group. Its discovery is generally attributed to Heinrich Gustav Magnus , who prepared it by the action of solid sulfur trioxide on ethanol in 1833. [ 1 ]
Tosylhydrazone salts can react with metals to form metal carbenes and used in cyclopropanations and epoxidations. [3] [4] An example of a transition metal-catalyzed cyclopropanation is a synthesis of tranylcypromine, [5] [6] in which the sodium salt of benzaldehyde tosylhydrazone is converted to a rhodium metal carbene through the diazo ...