2-Thiophenemethanamine, α-(phenylmethyl)-, hydrochloride (1:1), with CAS number 102339-13-9, is a chemical compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features an amine functional group, indicating its potential basicity and ability to form salts, as evidenced by its hydrochloride form. The presence of the phenylmethyl group suggests that it may exhibit significant hydrophobic characteristics, influencing its solubility and interaction with biological systems. As a hydrochloride salt, it is likely to be more soluble in water compared to its free base form, enhancing its utility in various applications, including pharmaceuticals. The compound may exhibit biological activity, potentially acting as a ligand or modulator in biochemical pathways, although specific pharmacological properties would require further investigation. Overall, its unique structural features position it as a compound of interest in both synthetic and medicinal chemistry contexts.

2-Thiophenemethanamine,a-(phenylmethyl)-, hydrochloride(1:1)

102339-13-9: 2-Thiophenemethanamine, α-(phenylmethyl)-, hydrochloride (1:1), with CAS number 102339-13-9, is a chemical compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features an amine functional group, indicating its potential basicity and ability to form salts, as evidenced by its hydrochloride form. The presence of the phenylmethyl group suggests that it may exhibit significant hydrophobic characteristics, influencing its solubility and interaction with biological systems. As a hydrochloride salt, it is likely to be more soluble in water compared to its free base form, enhancing its utility in various applications, including pharmaceuticals. The compound may exhibit biological activity, potentially acting as a ligand or modulator in biochemical pathways, although specific pharmacological properties would require further investigation. Overall, its unique structural features position it as a compound of interest in both synthetic and medicinal chemistry contexts.

CAS 102339-13-9

2-Thiophenemethanamine,a-(phenylmethyl)-, hydrochloride(1:1)

2-Phenyl-1-(thiophen-2-yl)ethan-1-amine hydrochloride

Ref: 3D-CEA33913