886055-59-0

Basic information

• Product Name: (R,R)-N-(3,5-di-tert-butylsalicylidene)-N'-[3-tert-butyl-5-(4'-hydroxyphenylethynyl)salicylidene]-1,2-cyclohexanediamine
• Synonyms: (R,R)-N-(3,5-di-tert-butylsalicylidene)-N'-[3-tert-butyl-5-(4'-hydroxyphenylethynyl)salicylidene]-1,2-cyclohexanediamine
• CAS NO: 886055-59-0
• Molecular Weight: 606.849
• Mol File: 886055-59-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (R,R)-N-(3,5-di-tert-butylsalicylidene)-N'-[3-tert-butyl-5-(4'-hydroxyphenylethynyl)salicylidene]-1,2-cyclohexanediamine(CAS DataBase Reference)
• NIST Chemistry Reference: (R,R)-N-(3,5-di-tert-butylsalicylidene)-N'-[3-tert-butyl-5-(4'-hydroxyphenylethynyl)salicylidene]-1,2-cyclohexanediamine(886055-59-0)
• EPA Substance Registry System: (R,R)-N-(3,5-di-tert-butylsalicylidene)-N'-[3-tert-butyl-5-(4'-hydroxyphenylethynyl)salicylidene]-1,2-cyclohexanediamine(886055-59-0)

Safety Data

• Hazardous Substances Data: 886055-59-0(Hazardous Substances Data)

Upstream product

• 881538-06-3 3-tert-butyl-2-hydroxy-5-(4'-hydroxyphenylethynyl)benzaldehyde 
• 37942-07-7 3,5-di-tert-butyl-2-hydroxybenzaldehyde 
• 881538-10-9 5-trimethylsilylethynyl-3-tert-butyl-2-hydroxybenzaldehyde 
• 881538-09-6 3-tert-butyl-5-ethynyl-2-hydroxybenzaldehyde 
• 153759-58-1 5-bromo-3-tert-butyl-2-hydroxybenzaldehyde 
• 10323-39-4 4-bromo-2-tert-butylphenol 
• 88-18-6 2-tert-Butylphenol 
• 540-38-5 p-Iodophenol 
• 191480-63-4 (1R,2R)-1,2-diaminocyclohexane monohydrochloride 

Downstream Products

• 910481-25-3 Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid 4-{3-tert-butyl-5-[((E)-(1R,2R)-2-{[1-(3,5-di-tert-butyl-2-hydroxy-phenyl)-meth-(E)-ylidene]-amino}-cyclohexylimino)-methyl]-4-hydroxy-phenylethynyl}-phenyl ester 

Relevant articles and documents

A practical one-pot synthesis of enantiopure unsymmetrical salen ligands

A practical, one-pot synthesis of enantiopure unsymmetrical salen ligands is described, using a 1:1:1 molar ratio of a chiral diamine and two different salicylaldehydes. The new synthetic protocol can be readily performed in good yields (60-85%) on a mult

POLYMERIC SALEN COMPOUNDS AND METHODS THEREOF

The present disclosure provides a polymerizable compound of the formula (I) where the R1, R2, R’1, R’2, X1 to X8, Y1, Y2, M and L have any of values as defined in the