α-(1,1-Dimethylethyl)benzenemethanamine, also known as a substituted amine, is characterized by its structure, which features a benzene ring attached to a methanamine group, with a tert-butyl group (1,1-dimethylethyl) substituent. This compound typically exhibits properties associated with amines, such as basicity and the ability to form hydrogen bonds, which can influence its solubility in various solvents. The presence of the bulky tert-butyl group can affect its steric hindrance, potentially impacting its reactivity and interaction with other molecules. The compound may also display hydrophobic characteristics due to the non-polar nature of the tert-butyl group, which can influence its behavior in biological systems and industrial applications. Additionally, α-(1,1-Dimethylethyl)benzenemethanamine may have implications in organic synthesis and could serve as a precursor or intermediate in the production of more complex chemical entities. Safety data should be consulted for handling and usage, as with all chemical substances.

α-(1,1-Dimethylethyl)benzenemethanamine

61501-04-0: 2,2-Dimethyl-1-Phenyl-Propylamine, 2,2-Dimethyl-1-phenylpropylamine, Benzenemethanamine, Α-(1,1-Dimethylethyl)-, Benzylamine, α-tert-butyl-, α-(1,1-Dimethylethyl)benzenemethanamine, α-tert-Butylbenzylamine, ω-Phenyl-tert-butyl-methylamine

2,2-Dimethyl-1-phenyl-propylamine

2,2-Dimethyl-1-phenylpropylamine

2,2-Dimethyl-1-phenyl-propylamine is a chiral molecule that is synthesized in two steps. First, an imine is formed by reacting a phenyl ring with an amino acid derived from the 2,2-dimethylbenzaldehyde. The second step involves the use of a biocatalyst to form an asymmetric synthesis of the racemic mixture using carbonyl as the leaving group and one of three different alkylating agents. The product then undergoes hydrogenation to yield the desired enantiomer (S) and (R). This compound has been found to have reactive properties due to its ability to form hydrogen bonds and its conformation.

CAS 61501-04-0: α-(1,1-Dimethylethyl)benzenemethanamine

2,2-Dimethyl-1-phenyl-propylamine

Ref: 54-OR904924

2,2-Dimethyl-1-phenylpropylamine

Ref: 10-F078663

2,2-Dimethyl-1-phenyl-propylamine

Ref: 3D-FD142671

2,2-Dimethyl-1-phenylpropan-1-amine

Ref: IN-DA003FBC