S-N,N-Dimethyl-[1,1'-binaphthalene]-2,2'-diamine, with the CAS number 921212-80-8, is an organic compound characterized by its unique binaphthalene structure, which consists of two naphthalene units connected by a single bond. This compound features two amino groups (–NH2) at the 2,2' positions of the binaphthalene framework, each of which is further substituted with two methyl groups (–CH3), resulting in the dimethylation of the amine functionalities. The presence of these functional groups imparts specific chemical properties, such as increased solubility in organic solvents and potential reactivity in various chemical reactions, including those involving nucleophilic substitution or coupling reactions. The stereochemistry of the binaphthalene core can lead to interesting chiral properties, making this compound of interest in asymmetric synthesis and catalysis. Additionally, its structural characteristics may contribute to its potential applications in materials science, organic electronics, or as a ligand in coordination chemistry. Overall, S-N,N-dimethyl-[1,1'-binaphthalene]-2,2'-diamine is a versatile compound with significant implications in both synthetic and applied chemistry.

S-N,N-diMethyl-[1,1'-Binaphthalene]-2,2'-diaMine

921212-80-8: S-N,N-Dimethyl-[1,1'-binaphthalene]-2,2'-diamine, with the CAS number 921212-80-8, is an organic compound characterized by its unique binaphthalene structure, which consists of two naphthalene units connected by a single bond. This compound features two amino groups (–NH2) at the 2,2' positions of the binaphthalene framework, each of which is further substituted with two methyl groups (–CH3), resulting in the dimethylation of the amine functionalities. The presence of these functional groups imparts specific chemical properties, such as increased solubility in organic solvents and potential reactivity in various chemical reactions, including those involving nucleophilic substitution or coupling reactions. The stereochemistry of the binaphthalene core can lead to interesting chiral properties, making this compound of interest in asymmetric synthesis and catalysis. Additionally, its structural characteristics may contribute to its potential applications in materials science, organic electronics, or as a ligand in coordination chemistry. Overall, S-N,N-dimethyl-[1,1'-binaphthalene]-2,2'-diamine is a versatile compound with significant implications in both synthetic and applied chemistry.

<p>(S)-N,N-Dimethyl-[1,1'-binaphthalene]-2,2'-diamine</p>

CAS 921212-80-8

S-N,N-diMethyl-[1,1'-Binaphthalene]-2,2'-diaMine

(S)-N,N-Dimethyl-[1,1'-binaphthalene]-2,2'-diamine

Ref: 54-OR1059503