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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 .
Dibenzylamine is an organic compound with the formula (C 6 H 5 CH 2) 2 NH.It is classified as a secondary amine, being the middle member of the series that includes the primary amine benzylamine (C 6 H 5 CH 2 NH 2) and the tertiary amine tribenzylamine ((C 6 H 5 CH 2) 3 N).
The ratio of 15 N to 14 N is of relevance because in most biological contexts, 14 N is preferentially uptaken as the lighter isotope. As a result, samples enriched in 15 N can often be introduced through a non-biological context.
N,N-Dimethylbenzylamine can be synthesized by the Eschweiler–Clarke reaction of benzylamine [2] [3] Reactions
N-isopropylbenzylamine is a compound that has appeared in chemical literature often playing an intermediary role in applications of experimental synthesis and novel organic transformations.
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1-Phenylethylamine may be prepared by the reductive amination of acetophenone: [1]. C 6 H 5 C(O)CH 3 + NH 3 + H 2 → C 6 H 5 CH(NH 2)CH 3 + H 2 O. The Leuckart reaction, using ammonium formate, is another method for this transformation.
Xylamine is a monoaminergic neurotoxin and benzylamine derivative that is closely related to DSP-4. [1] [2] It is a relatively selective noradrenergic neurotoxin, which is attributed to its high affinity for the norepinephrine transporter (NET). [1]