N,N-Dimethyl-N'-(thiophen-3-ylmethyl)ethane-1,2-diamine is an organic compound characterized by its amine functional groups and a thiophene ring, which contributes to its unique chemical properties. This compound features two primary amine groups, which can participate in hydrogen bonding and may influence its solubility and reactivity. The presence of the thiophene moiety, a five-membered aromatic ring containing sulfur, imparts additional electronic characteristics, potentially enhancing its interactions in biological systems or with other chemical entities. The dimethyl substitution on the nitrogen atoms affects steric hindrance and can influence the compound's overall stability and reactivity. This substance may exhibit interesting pharmacological properties, making it a candidate for research in medicinal chemistry. Its molecular structure suggests potential applications in various fields, including organic synthesis and materials science. As with many amines, it may also be sensitive to oxidation and can participate in various chemical reactions, including alkylation and acylation, making it a versatile building block in organic synthesis.

N,N-dimethyl-N'-(thiophen-3-ylmethyl)ethane-1,2-diamine

892593-13-4: N,N-Dimethyl-N'-(thiophen-3-ylmethyl)ethane-1,2-diamine is an organic compound characterized by its amine functional groups and a thiophene ring, which contributes to its unique chemical properties. This compound features two primary amine groups, which can participate in hydrogen bonding and may influence its solubility and reactivity. The presence of the thiophene moiety, a five-membered aromatic ring containing sulfur, imparts additional electronic characteristics, potentially enhancing its interactions in biological systems or with other chemical entities. The dimethyl substitution on the nitrogen atoms affects steric hindrance and can influence the compound's overall stability and reactivity. This substance may exhibit interesting pharmacological properties, making it a candidate for research in medicinal chemistry. Its molecular structure suggests potential applications in various fields, including organic synthesis and materials science. As with many amines, it may also be sensitive to oxidation and can participate in various chemical reactions, including alkylation and acylation, making it a versatile building block in organic synthesis.

CAS 892593-13-4

N,N-dimethyl-N'-(thiophen-3-ylmethyl)ethane-1,2-diamine

[2-(dimethylamino)ethyl][(thiophen-3-yl)methyl]amine

Ref: IN-DA0041YZ

N,N-Dimethyl-N'-(thiophen-3-ylmethyl)ethane-1,2-diamine

Ref: 3D-SKB59313