C-(5,6,7,8-Tetrahydro-naphthalen-2-yl)-methylamine, with the CAS number 15402-69-4, is an organic compound characterized by its tetrahydronaphthalene structure, which consists of a bicyclic system featuring a saturated naphthalene ring. This compound contains a methylamine functional group, indicating the presence of an amine (-NH2) attached to a methyl group. The tetrahydronaphthalene moiety contributes to its hydrophobic characteristics, while the amine group introduces basicity and potential for hydrogen bonding. This compound may exhibit biological activity, making it of interest in medicinal chemistry and pharmacology. Its solubility properties are likely influenced by the balance between the hydrophobic naphthalene structure and the polar amine group. Additionally, the compound's reactivity can be attributed to the presence of the amine, which can participate in various chemical reactions, including alkylation and acylation. Overall, C-(5,6,7,8-Tetrahydro-naphthalen-2-yl)-methylamine is a versatile compound with potential applications in various fields, including drug development and organic synthesis.

C-(5,6,7,8-TETRAHYDRO-NAPHTHALEN-2-YL)-METHYLAMINE

15402-69-4: C-(5,6,7,8-Tetrahydro-naphthalen-2-yl)-methylamine, with the CAS number 15402-69-4, is an organic compound characterized by its tetrahydronaphthalene structure, which consists of a bicyclic system featuring a saturated naphthalene ring. This compound contains a methylamine functional group, indicating the presence of an amine (-NH2) attached to a methyl group. The tetrahydronaphthalene moiety contributes to its hydrophobic characteristics, while the amine group introduces basicity and potential for hydrogen bonding. This compound may exhibit biological activity, making it of interest in medicinal chemistry and pharmacology. Its solubility properties are likely influenced by the balance between the hydrophobic naphthalene structure and the polar amine group. Additionally, the compound's reactivity can be attributed to the presence of the amine, which can participate in various chemical reactions, including alkylation and acylation. Overall, C-(5,6,7,8-Tetrahydro-naphthalen-2-yl)-methylamine is a versatile compound with potential applications in various fields, including drug development and organic synthesis.

CAS 15402-69-4

C-(5,6,7,8-TETRAHYDRO-NAPHTHALEN-2-YL)-METHYLAMINE

(5,6,7,8-Tetrahydronaphthalen-2-yl)methanamine

Ref: 54-OR1044729

(5,6,7,8-tetrahydronaphthalen-2-yl)methanamine

Ref: 3D-QAA40269