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  2. Cyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylamine

    Cyclohexylamine is used as an intermediate in synthesis of other organic compounds. It is the precursor to sulfenamide -based reagents used as accelerators for vulcanization. The amine itself is an effective corrosion inhibitor. It has been used as a flushing aid in the printing ink industry. [5]

  3. Arylcyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Arylcyclohexylamine

    An arylcyclohexylamine is composed of a cyclohexylamine unit with an aryl moiety attachment. The aryl group is positioned geminal to the amine. In the simplest cases, the aryl moiety is typically a phenyl ring, sometimes with additional substitution. The amine is usually not primary; secondary amines such as methylamine or ethylamine, or ...

  4. Eticyclidine - Wikipedia

    en.wikipedia.org/wiki/Eticyclidine

    Eticyclidine. Eticyclidine ( PCE, CI-400) is a dissociative anesthetic drug with hallucinogenic effects. It is similar in effects to phencyclidine but is slightly more potent. PCE was developed by Parke-Davis in the 1970s and evaluated for anesthetic potential under the code name CI-400, [2] but research into PCE was not continued after the ...

  5. Phencyclidine - Wikipedia

    en.wikipedia.org/wiki/Phencyclidine

    Phencyclidine or phenylcyclohexyl piperidine ( PCP ), also known in its use as a street drug as angel dust among other names, is a dissociative anesthetic mainly used recreationally for its significant mind-altering effects. [1] [5] PCP may cause hallucinations, distorted perceptions of sounds, and violent behavior.

  6. List of Feynman diagrams - Wikipedia

    en.wikipedia.org/wiki/List_of_Feynman_diagrams

    In the Stückelberg–Feynman interpretation, pair annihilation is the same process as pair production. Møller scattering. electron-electron scattering. Bhabha scattering. electron-positron scattering. Penguin diagram. a quark changes flavor via a W or Z loop. Tadpole diagram. One loop diagram with one external leg.

  7. Ei mechanism - Wikipedia

    en.wikipedia.org/wiki/Ei_mechanism

    mechanism. In organic chemistry, the Ei mechanism ( Elimination Internal/Intramolecular ), also known as a thermal syn elimination or a pericyclic syn elimination, is a special type of elimination reaction in which two vicinal (adjacent) substituents on an alkane framework leave simultaneously via a cyclic transition state to form an alkene in ...

  8. Combinatorial chemistry - Wikipedia

    en.wikipedia.org/wiki/Combinatorial_chemistry

    Combinatorial chemistry. Combinatorial chemistry comprises chemical synthetic methods that make it possible to prepare a large number (tens to thousands or even millions) of compounds in a single process. These compound libraries can be made as mixtures, sets of individual compounds or chemical structures generated by computer software. [1]

  9. Phenyl group - Wikipedia

    en.wikipedia.org/wiki/Phenyl_group

    Phenyl group. In organic chemistry, the phenyl group, or phenyl ring, is a cyclic group of atoms with the formula C6H5, and is often represented by the symbol Ph (archaically φ ). The phenyl group is closely related to benzene and can be viewed as a benzene ring, minus a hydrogen, which may be replaced by some other element or compound to ...