1341198-17-1

Basic information

• Product Name: [4-(4-tert-butylphenyl)-2-isopropyl-1H-inden-1-yl](dimethyl)(2-methyl-4-phenyl-1,5,6,7-tetrahydro-s-indacen-1-yl)silane
• Synonyms: [4-(4-tert-butylphenyl)-2-isopropyl-1H-inden-1-yl](dimethyl)(2-methyl-4-phenyl-1,5,6,7-tetrahydro-s-indacen-1-yl)silane
• CAS NO: 1341198-17-1
• Molecular Weight: 592.94
• Mol File: 1341198-17-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [4-(4-tert-butylphenyl)-2-isopropyl-1H-inden-1-yl](dimethyl)(2-methyl-4-phenyl-1,5,6,7-tetrahydro-s-indacen-1-yl)silane(CAS DataBase Reference)
• NIST Chemistry Reference: [4-(4-tert-butylphenyl)-2-isopropyl-1H-inden-1-yl](dimethyl)(2-methyl-4-phenyl-1,5,6,7-tetrahydro-s-indacen-1-yl)silane(1341198-17-1)
• EPA Substance Registry System: [4-(4-tert-butylphenyl)-2-isopropyl-1H-inden-1-yl](dimethyl)(2-methyl-4-phenyl-1,5,6,7-tetrahydro-s-indacen-1-yl)silane(1341198-17-1)

Safety Data

• Hazardous Substances Data: 1341198-17-1(Hazardous Substances Data)

Upstream product

• 656800-69-0 3,5,6,7-tetrahydro-2-methyl-4-phenyl-s-hydraindacen-1(2H)-ol 
• 538328-62-0 [4-(4-tert-butylphenyl)-2-isopropyl-1H-inden-1-yl](chloro)dimethylsilane 
• 852160-02-2 6-methyl-4-phenyl-1,2,3,5-tetrahydro-s-indacene 
• 656800-67-8 4-bromo-2-methyl-3,5,6,7-tetrahydro-s-indacen-1(2H)-one 
• 656800-68-9 4-phenyl-2-methyl-3,5,6,7-tetrahydro-s-indacen-1(2H)-one 
• 496-11-7 INDANE 
• 202667-44-5 2-methyl-3,5,6,7-tetrahydro-s-indacen-1(2H)-one 
• 98-80-6 phenylboronic acid 

Downstream Products

• 1033598-91-2 μ-dimethylsylilene[η5-4-(4-tert-butylphenyl)-2-isopropyl-1H-inden-1-yl](η5-2-methyl-4-phenyl-1,5,6,7-tetrahydro-s-indacen-1-yl)dichlorozirconium(IV) 

Relevant articles and documents

Asymmetric ansa-zirconocenes containing a 2-methyl-4-aryltetrahydroindacene fragment: Synthesis, structure, and catalytic activity in propylene polymerization and copolymerization

A set of asymmetric bis-indenyl zirconium SiMe2-bridged ansa-complexes, containing 2-isopropyl-4-arylindenyl and 2-methyl-4- aryltetrahydroindacenyl fragments, have been synthesized. These complexes demonstrate better catalytic activity, stereoselectivty, and polymer molecular weight capability in propylene homo-and copolymerization in comparison to analogues without a tetrahydroindacenyl fragment.