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  2. Phenylbiguanide - Wikipedia

    en.wikipedia.org/wiki/Phenylbiguanide

    Phenylbiguanide (PBG) is a 5-HT3 agonist used to study the role of 5-HT3 receptors in the central nervous system. [1] It has been found to trigger dopamine release in the nucleus accumbens of rats. [2]

  3. Biguanide - Wikipedia

    en.wikipedia.org/wiki/Biguanide

    Biguanide (/ b aɪ ˈ ɡ w ɒ n aɪ d /) is the organic compound with the formula HN(C(NH)NH 2) 2. It is a colorless solid that dissolves in water to give a highly basic solution. It is a colorless solid that dissolves in water to give a highly basic solution.

  4. Sigma bond - Wikipedia

    en.wikipedia.org/wiki/Sigma_bond

    There is no more than 1 sigma bond between any two atoms. Molecules with rings have additional sigma bonds, such as benzene rings, which have 6 C−C sigma bonds within the ring for 6 carbon atoms. The anthracene molecule, C 14 H 10, has three rings so that the rule gives the number of sigma bonds as 24 + 3 − 1 = 26. In this case there are 16 ...

  5. (Bis(trifluoroacetoxy)iodo)benzene - Wikipedia

    en.wikipedia.org/wiki/(Bis(trifluoroacetoxy)iodo...

    The reaction can also be carried out under mildly acidic conditions by way of the same intermediate using a hypervalent iodine compound in aqueous solution. [1] An example published in Organic Syntheses is the conversion of cyclobutanecarboxamide , easily synthesized from cyclobutylcarboxylic acid , to cyclobutylamine . [ 2 ]

  6. Chlorophenylbiguanide - Wikipedia

    en.wikipedia.org/wiki/Chlorophenylbiguanide

    meta-Chlorophenylbiguanide (1-(3-Chlorophenylbiguanide, m-CPBG) is an allosteric agonist and modulator of the 5-HT 3 receptor [1] [2] [3] and an antagonist of the α 2A-adrenergic receptor. [4] It has anxiogenic , emetic and hypothermic effects in animal studies.

  7. Stevens rearrangement - Wikipedia

    en.wikipedia.org/wiki/Stevens_rearrangement

    The original 1928 publication by Thomas S. Stevens [2] concerned the reaction of 1-phenyl-2-(N,N-dimethylamino)ethanone with benzyl bromide to the ammonium salt followed by the rearrangement reaction with sodium hydroxide in water to the rearranged amine. Stevens rearrangement 1928. A 1932 publication [3] described the corresponding sulfur ...

  8. Hydrazines - Wikipedia

    en.wikipedia.org/wiki/Hydrazines

    Hydrazines (R 2 N−NR 2) are a class of chemical compounds with two nitrogen atoms linked via a covalent bond and which carry from one up to four alkyl or aryl substituents. Hydrazines can be considered as derivatives of the inorganic hydrazine (H 2 N−NH 2), in which one or more hydrogen atoms have been replaced by hydrocarbon groups. [1]

  9. Phenyl group - Wikipedia

    en.wikipedia.org/wiki/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) or Ø. 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 serve as a ...

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