210036-17-2

Basic information

• Product Name: 6,6'-Bis-(3,5-bis-benzyloxy-benzyloxy)-2,2'-bis-triisopropylsilanyloxy-[1,1']binaphthalenyl
• Synonyms: 6,6'-Bis-(3,5-bis-benzyloxy-benzyloxy)-2,2'-bis-triisopropylsilanyloxy-[1,1']binaphthalenyl
• CAS NO: 210036-17-2
• Molecular Weight: 1235.76
• Mol File: 210036-17-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6,6'-Bis-(3,5-bis-benzyloxy-benzyloxy)-2,2'-bis-triisopropylsilanyloxy-[1,1']binaphthalenyl(CAS DataBase Reference)
• NIST Chemistry Reference: 6,6'-Bis-(3,5-bis-benzyloxy-benzyloxy)-2,2'-bis-triisopropylsilanyloxy-[1,1']binaphthalenyl(210036-17-2)
• EPA Substance Registry System: 6,6'-Bis-(3,5-bis-benzyloxy-benzyloxy)-2,2'-bis-triisopropylsilanyloxy-[1,1']binaphthalenyl(210036-17-2)

Safety Data

• Hazardous Substances Data: 210036-17-2(Hazardous Substances Data)

Upstream product

• 24131-32-6 3,5-bis(benzyloxy)benzyl bromide 
• 312911-15-2 2,2'-Bis-triisopropylsilanyloxy-[1,1']binaphthalenyl-6,6'-diol 
• 13154-24-0 triisopropylsilyl chloride 
• 79082-80-7 (S)-6,6'-dibromo-1,1'-binaphthalene-2,2'-diol 
• 312911-14-1 6,6'-Dibromo-2,2'-bis-triisopropylsilanyloxy-[1,1']binaphthalenyl 

Relevant articles and documents

Synthesis of optically active dendritic binaphtols and their metal complexes for asymmetric catalysis

Optically active binaphthols bearing substituents at the 6,6-positions were synthesized by the base reaction of 6,6'-dihydroxyl-2,2'-binaphthol and the dendritic benzyl bromides. Despite the bulky dendritic substituents, the dendritic binaphthols were found to from metal complexes and catalyze asymmetric C-C bond forming reactions.