Benzenebutanamine, α-methyl- (CAS 22148-82-9) is an organic compound that belongs to the class of amines and is characterized by the presence of both a benzene ring and a butylamine group. The structure features a butyl chain with a methyl group attached to the alpha position relative to the amine functional group. This compound is typically a colorless to pale yellow liquid or solid, depending on its specific form and purity. It is known for its potential applications in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. The presence of the aromatic benzene ring contributes to its stability and hydrophobic characteristics, while the amine group can participate in hydrogen bonding, influencing its solubility in different solvents. Safety data indicates that, like many amines, it may be irritating to the skin and eyes, and appropriate handling precautions should be taken. Overall, benzenebutanamine, α-methyl- is a compound of interest in both industrial and research settings.

Benzenebutanamine, a-methyl-

22148-82-9: Benzenebutanamine, a-methyl-, (?à)-, Butylamine, 1-methyl-4-phenyl-, (?à)- (8CI)

1-Methyl-4-phenylbutylamine

1-Methyl-4-phenyl-butylamine is an organic compound that reacts with Grignard reagents to form cyclohexenimines. It can also be used in the synthesis of aziridines, which are useful as a type of nucleophile. This chemical is regiospecifically produced by refluxing a mixture of ethylmagnesium bromide and cyclohexene hydrochloride in hydrochloric acid. The ring-opening reaction of 1-methyl-4-phenylbutanamine yields diethyl aminomalonate, which can be converted into malonic esters and other compounds.

CAS 22148-82-9: Benzenebutanamine, a-methyl-

1-Methyl-4-phenylbutylamine

Ref: 10-F038414

1-Methyl-4-phenyl-butylamine

Ref: 3D-XAA14882