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  2. Dimethylbenzylamine - Wikipedia

    en.wikipedia.org/wiki/Dimethylbenzylamine

    Dimethylbenzylamine is the organic compound with the formula C 6 H 5 CH 2 N(CH 3) 2. The molecule consists of a benzyl group, C 6 H 5 CH 2 , attached to a dimethyl amino functional group . It is a colorless liquid.

  3. Benzylamine - Wikipedia

    en.wikipedia.org/wiki/Benzylamine

    Benzylamine, also known as phenylmethylamine, is an organic chemical compound with the condensed structural formula C 6 H 5 CH 2 NH 2 (sometimes abbreviated as PhCH 2 NH 2 or BnNH 2).It consists of a benzyl group, C 6 H 5 CH 2, attached to an amine functional group, NH 2.

  4. BTX (chemistry) - Wikipedia

    en.wikipedia.org/wiki/BTX_(chemistry)

    The xylene isomers are distinguished by the designations ortho – (or o –), meta – (or m –), and para ... Molecular formula: C 6 H 6: C 7 H 8: C 8 H 10:

  5. PCB congener list - Wikipedia

    en.wikipedia.org/wiki/PCB_congener_list

    Congener descriptors give a shorthand notation for geometry and substituent positions. The twelve congeners that display all four of the descriptors are referred to as being "dioxin-like", referring both to their toxicity and structural features which make them similar to 2,3,7,8-tetrachlorodibenzo-p-dioxin (2378-TCDD). [1]

  6. Spin isomers of hydrogen - Wikipedia

    en.wikipedia.org/wiki/Spin_isomers_of_hydrogen

    The ratio between numbers of ortho and para molecules is about 3:1 at standard temperature where many rotational energy levels are populated, favoring the ortho form as a result of thermal energy. However, at low temperatures only the J = 0 level is appreciably populated, so that the para form dominates at low temperatures (approximately 99.8% ...

  7. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    In organic chemistry, benzyl is the substituent or molecular fragment possessing the structure R−CH 2 −C 6 H 5. Benzyl features a benzene ring ( C 6 H 6 ) attached to a methylene group ( −CH 2 − ).

  8. Directed ortho metalation - Wikipedia

    en.wikipedia.org/wiki/Directed_ortho_metalation

    Directed ortho metalation (DoM) is an adaptation of electrophilic aromatic substitution in which electrophiles attach themselves exclusively to the ortho-position of a direct metalation group or DMG through the intermediary of an aryllithium compound. [1] The DMG interacts with lithium through a hetero atom.

  9. Orthomolecular medicine - Wikipedia

    en.wikipedia.org/wiki/Orthomolecular_medicine

    American chemist Linus Pauling coined the term "orthomolecular" in the 1960s to mean "the right molecules in the right amounts" (ortho-in Greek implies "correct"). [11] Proponents of orthomolecular medicine hold that treatment must be based on each patient's individual biochemistry. [12] [13]