169179-44-6

Basic information

• Product Name: 11'-(tert-butyl)-5',17',23',35',38',40'43',45'-octamethyldispiro[cyclohexane-1,2'-[7,15,25,33]tetraazaheptacyclo[32.2.2.2.2(3,6).2(16,19).2(21,24).1(3,13).1(27,31)]hexatetraconta[3,5,9,11,13⁽⁴⁴⁾,16,18,21,23,27,29,31⁽³⁹⁾,34,36,37,40,42,45]octadecaene..].
• Synonyms: 11'-(tert-butyl)-5',17',23',35',38',40'43',45'-octamethyldispiro[cyclohexane-1,2'-[7,15,25,33]tetraazaheptacyclo[32.2.2.2.2(3,6).2(16,19).2(21,24).1(3,13).1(27,31)]hexatetraconta[3,5,9,11,13⁽⁴⁴⁾,16,18,21,23,27,29,31⁽³⁹⁾,34,36,37,40,42,45]octadecaene..].
• CAS NO: 169179-44-6
• Molecular Weight: 961.3
• Mol File: 169179-44-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 11'-(tert-butyl)-5',17',23',35',38',40'43',45'-octamethyldispiro[cyclohexane-1,2'-[7,15,25,33]tetraazaheptacyclo[32.2.2.2.2(3,6).2(16,19).2(21,24).1(3,13).1(27,31)]hexatetraconta[3,5,9,11,13⁽⁴⁴⁾,16,18,21,23,27,29,31⁽³⁹⁾,34,36,37,40,42,45]octadecaene..].(CAS DataBase Reference)
• NIST Chemistry Reference: 11'-(tert-butyl)-5',17',23',35',38',40'43',45'-octamethyldispiro[cyclohexane-1,2'-[7,15,25,33]tetraazaheptacyclo[32.2.2.2.2(3,6).2(16,19).2(21,24).1(3,13).1(27,31)]hexatetraconta[3,5,9,11,13⁽⁴⁴⁾,16,18,21,23,27,29,31⁽³⁹⁾,34,36,37,40,42,45]octadecaene..].(169179-44-6)
• EPA Substance Registry System: 11'-(tert-butyl)-5',17',23',35',38',40'43',45'-octamethyldispiro[cyclohexane-1,2'-[7,15,25,33]tetraazaheptacyclo[32.2.2.2.2(3,6).2(16,19).2(21,24).1(3,13).1(27,31)]hexatetraconta[3,5,9,11,13⁽⁴⁴⁾,16,18,21,23,27,29,31⁽³⁹⁾,34,36,37,40,42,45]octadecaene..].(169179-44-6)

Safety Data

• Hazardous Substances Data: 169179-44-6(Hazardous Substances Data)

Downstream Products

• 199794-01-9 N,N'-bis<4-(triphenylmethyl)phenyl>fumardiamide 

Relevant articles and documents

Rotaxane or pseudorotaxane? Effects of small structural variations on the deslipping kinetics of rotaxanes with stopper groups of intermediate size

Three series of rotaxanes have been synthesized variously by slipping synthesis, in which axis and wheel are melted in admixture, by recognition of amide groups inside the macrocyclic wheel, or by an anionic template method, in which the stoppering phenol