6,7-Dimethoxy-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene, identified by its CAS number 22825-00-9, is an organic compound characterized by its complex structure, which includes a naphthalene core with multiple methyl and methoxy substituents. This compound features two methoxy groups located at the 6 and 7 positions of the naphthalene ring, contributing to its chemical reactivity and solubility properties. The presence of four methyl groups at the 1, 1, 4, and 4 positions enhances its steric bulk and may influence its physical properties, such as boiling point and melting point. Typically, compounds of this nature exhibit hydrophobic characteristics due to their hydrocarbon framework, making them less soluble in water but more soluble in organic solvents. Additionally, the methoxy groups can participate in various chemical reactions, including methylation and ether formation. This compound may have applications in organic synthesis, materials science, or as a potential intermediate in the production of more complex molecules. However, specific applications and biological activities would require further investigation.

6,7-dimethoxy-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene

22825-00-9: 6,7-Dimethoxy-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene, identified by its CAS number 22825-00-9, is an organic compound characterized by its complex structure, which includes a naphthalene core with multiple methyl and methoxy substituents. This compound features two methoxy groups located at the 6 and 7 positions of the naphthalene ring, contributing to its chemical reactivity and solubility properties. The presence of four methyl groups at the 1, 1, 4, and 4 positions enhances its steric bulk and may influence its physical properties, such as boiling point and melting point. Typically, compounds of this nature exhibit hydrophobic characteristics due to their hydrocarbon framework, making them less soluble in water but more soluble in organic solvents. Additionally, the methoxy groups can participate in various chemical reactions, including methylation and ether formation. This compound may have applications in organic synthesis, materials science, or as a potential intermediate in the production of more complex molecules. However, specific applications and biological activities would require further investigation.

<p>6,7-Dimethoxy-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene, 99+% Redox shuttle ANL-RS21</p>

CAS 22825-00-9

6,7-dimethoxy-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene

6,7-Dimethoxy-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene, 99+% Redox shuttle ANL-RS21

Ref: 08-08-0220