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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.
Diphenylamine is an organic compound with the formula (C 6 H 5) 2 NH. The compound is a derivative of aniline, consisting of an amine bound to two phenyl groups. The compound is a colorless solid, but commercial samples are often yellow due to oxidized impurities. [5]
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dibenzylamine: 103-49-1 C 14 H 15 OP: ethyldiphenylphosphine oxide: 1733-57-9 C 14 H 15 O 2 P: methoxymethyldiphenylphosphine oxide: 4455-77-0 C 14 H 15 O 2 PS 2: edifenphos: 17109-49-8 C 14 H 15 O 3 P: dibenzyl phosphite: 17176-77-1 C 14 H 16: chamazulene: 529-05-5 C 14 H 16: eudalene: 490-65-3 C 14 H 16 ClN 3 O 4 S 2: cyclothiazide: 2259-96-3 ...
Dibenzylaniline or N,N-Dibenzylaniline is a chemical compound consisting of aniline with two benzyl groups as substituents on the nitrogen.. The substance crystallizes in the monoclinic crystal system.
The molecule consists of a nitrogen atom with two methyl substituents and one hydrogen.Dimethylamine is a weak base and the pKa of the ammonium CH 3-NH + 2-CH 3 is 10.73, a value above methylamine (10.64) and trimethylamine (9.79).
Tris(dibenzylideneacetone)dipalladium(0) or [Pd 2 (dba) 3] is an organopalladium compound.The compound is a complex of palladium(0) with dibenzylideneacetone (dba). It is a dark-purple/brown solid, which is modestly soluble in organic solvents.
In organic chemistry, the Buchwald–Hartwig amination is a chemical reaction for the synthesis of carbon–nitrogen bonds via the palladium-catalyzed coupling reactions of amines with aryl halides. [1]