6-(Chloromethyl)-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene, with the CAS number 163117-71-3, is an organic compound characterized by its complex structure, which includes a naphthalene core with multiple methyl groups and a chloromethyl substituent. This compound is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity. It exhibits hydrophobic properties due to its hydrocarbon framework, making it less soluble in water but more soluble in organic solvents. The presence of the chloromethyl group introduces reactivity, allowing for potential further chemical modifications, such as nucleophilic substitution reactions. Its unique structure may impart specific physical properties, such as a distinct boiling point and melting point, which are influenced by the steric hindrance from the tetramethyl groups. This compound may find applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals, due to its reactive chloromethyl group and stable naphthalene backbone. Safety data should be consulted for handling and storage, as chlorinated compounds can pose health risks.

6-(chloromethyl)-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene

163117-71-3: 6-(Chloromethyl)-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene, with the CAS number 163117-71-3, is an organic compound characterized by its complex structure, which includes a naphthalene core with multiple methyl groups and a chloromethyl substituent. This compound is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity. It exhibits hydrophobic properties due to its hydrocarbon framework, making it less soluble in water but more soluble in organic solvents. The presence of the chloromethyl group introduces reactivity, allowing for potential further chemical modifications, such as nucleophilic substitution reactions. Its unique structure may impart specific physical properties, such as a distinct boiling point and melting point, which are influenced by the steric hindrance from the tetramethyl groups. This compound may find applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals, due to its reactive chloromethyl group and stable naphthalene backbone. Safety data should be consulted for handling and storage, as chlorinated compounds can pose health risks.

CAS 163117-71-3

6-(chloromethyl)-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene

6-(Chloromethyl)-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene

Ref: IN-DA001TS3

6-(chloromethyl)-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene

Ref: 54-OR30104