Search results
Results from the WOW.Com Content Network
2-bromo-1-(4-methylphenyl)propan-1-one substituted cathinones and substituted amphetamines: 2-bromo-1-phenylpentan-1-one substituted cathinones and substituted amphetamines: 2-bromo-1-phenylpropan-1-one substituted cathinones and substituted amphetamines: BMK glycidic acid and esters methamphetamine 3-oxo-2-phenylbutanoic acid and its esters
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.
If there are multiple functional groups of the same type, either prefixed or suffixed, the position numbers are ordered numerically (thus ethane-1,2-diol, not ethane-2,1-diol.) The N position indicator for amines and amides comes before "1", e.g., CH 3 CH(CH 3)CH 2 NH(CH 3) is N,2-dimethylpropanamine.
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 dimethylamino functional group. It is a colorless liquid. It is used as a catalyst for the formation of polyurethane foams and epoxy resins.
Ethylamine, also known as ethanamine, is an organic compound with the formula CH 3 CH 2 NH 2. This colourless gas has a strong ammonia-like odor. It condenses just below room temperature to a liquid miscible with virtually all solvents. It is a nucleophilic base, as is typical for amines.
N,N'-Dimethylethylenediamine (DMEDA) is the organic compound with the formula (CH 3 NH) 2 C 2 H 4. It is a colorless liquid with a fishy odor. It features two secondary amine functional groups. Regarding its name, N and N' indicate that the methyl groups are attached to different nitrogen atoms.
Download QR code; Print/export Download as PDF; Printable version; ... Ethylmethylamine, or N-methylethanamine, is a compound with the chemical formula C 3 H 9 N.
Usually aminomethyl groups feature tertiary amines. Often they are obtained by alkylation with Eschenmoser's salt, a source of [CH 2 =N(CH 3) 2] +. A cobalt(III) complex of aminomethyl is known in the form [Co 2 (CH 2 NH 2)](ClO4) 2. [1] Aminomethyl is the first member of a series of 1-aminoalkyl groups of the form −(CH 2 −) n NH 2. [2]