2,2'-Dimethyl-1,1'-binaphthalene, with the CAS number 19634-89-0, is an organic compound characterized by its structure, which consists of two naphthalene units connected by a single bond, with two methyl groups attached to the 2-position of each naphthalene ring. This compound is a polycyclic aromatic hydrocarbon (PAH) and exhibits properties typical of such compounds, including a relatively high melting point and boiling point due to its planar structure and strong π-π stacking interactions. It is generally insoluble in water but soluble in organic solvents like benzene and toluene. The presence of methyl groups enhances its steric bulk, which can influence its reactivity and interactions with other molecules. 2,2'-Dimethyl-1,1'-binaphthalene is of interest in various fields, including materials science and organic chemistry, particularly in the study of chiral compounds and their applications in asymmetric synthesis. Its derivatives may also exhibit interesting optical properties, making them useful in the development of organic light-emitting diodes (OLEDs) and other electronic materials.

2,2'-dimethyl-1,1'-binaphthalene

19634-89-0: 2,2'-Dimethyl-1,1'-binaphthalene, with the CAS number 19634-89-0, is an organic compound characterized by its structure, which consists of two naphthalene units connected by a single bond, with two methyl groups attached to the 2-position of each naphthalene ring. This compound is a polycyclic aromatic hydrocarbon (PAH) and exhibits properties typical of such compounds, including a relatively high melting point and boiling point due to its planar structure and strong π-π stacking interactions. It is generally insoluble in water but soluble in organic solvents like benzene and toluene. The presence of methyl groups enhances its steric bulk, which can influence its reactivity and interactions with other molecules. 2,2'-Dimethyl-1,1'-binaphthalene is of interest in various fields, including materials science and organic chemistry, particularly in the study of chiral compounds and their applications in asymmetric synthesis. Its derivatives may also exhibit interesting optical properties, making them useful in the development of organic light-emitting diodes (OLEDs) and other electronic materials.

CAS 19634-89-0

2,2'-dimethyl-1,1'-binaphthalene

2,2'-DIMETHYLBIPHENYL

Ref: IN-DA00AQ64

(R)-2,2'-Dimethyl-1,1'-binaphthyl

Ref: 3B-D2837