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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.
The molecular formula C 9 H 13 N may refer to: Dimethylbenzylamine; Methylphenethylamines. Amphetamine (Benzedrine, Adderall) Dextroamphetamine; Levoamphetamine; β-Methylphenethylamine; N-Methylphenethylamine; 2-Methylphenethylamine; 3-Methylphenethylamine; 4-Methylphenethylamine; 2,4,6-Trimethylaniline
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.
N,N-Dimethylethylamine (DMEA), sometimes referred to as dimethylethylamine, is an organic compound with formula (CH 3) 2 NC 2 H 5.It is an industrial chemical that is mainly used in foundries as a catalyst for epoxy resins and polyurethane as well as sand core production.
The Sommelet–Hauser rearrangement (named after M. Sommelet [1] and Charles R. Hauser [2]) is a rearrangement reaction of certain benzyl quaternary ammonium salts. [3] [4] The reagent is sodium amide or another alkali metal amide and the reaction product a N,N-dialkylbenzylamine with a new alkyl group in the aromatic ortho position.
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N,N-dimethylbenzylamine undergoes cyclometalation readily by many transition metals. [16] A semi-practical implementations involve weakly coordinating directing groups, as illustrated by the Murai reaction. [17] Murai reaction; X = directing group.
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