1258276-28-6

Basic information

• Product Name: (11aS)-3,7-Bis[2,4,6-tris(1-methylethyl)phenyl]-10,11,12,13-tetrahydro-5-hydroxy-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin 5-oxide
• Synonyms: (11aS)-3,7-Bis[2,4,6-tris(1-methylethyl)phenyl]-10,11,12,13-tetrahydro-5-hydroxy-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin 5-oxide;(11aS)-10,11,12,13-tetrahydro-5-hydroxy-3,7-bis[2,4,6-tris(1-Methylethyl)phenyl]-5-oxide-Diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin;(11aS)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-bis[2,4,6- trisisopropylphenyl]-5-oxide-diindeno[7,1-de:1',7'-fg][1,3, 2]dioxaphosphocin;(11aS)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-bis[2,4,6-trisisopropylphenyl]-5-oxide-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin,99%e.e.
• CAS NO: 1258276-28-6
• Molecular Formula: C₄₇H₅₉O₄P
• Molecular Weight: 719.950661
• Mol File: 1258276-28-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 749.7±70.0 °C(Predicted)
• Appearance: /
• Density: 1.16±0.1 g/cm3 (20 ºC 760 Torr)
• PKA: 1.15±0.20(Predicted)
• CAS DataBase Reference: (11aS)-3,7-Bis[2,4,6-tris(1-methylethyl)phenyl]-10,11,12,13-tetrahydro-5-hydroxy-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin 5-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: (11aS)-3,7-Bis[2,4,6-tris(1-methylethyl)phenyl]-10,11,12,13-tetrahydro-5-hydroxy-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin 5-oxide(1258276-28-6)
• EPA Substance Registry System: (11aS)-3,7-Bis[2,4,6-tris(1-methylethyl)phenyl]-10,11,12,13-tetrahydro-5-hydroxy-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin 5-oxide(1258276-28-6)

Safety Data

• Hazardous Substances Data: 1258276-28-6(Hazardous Substances Data)

Usage

General Description

(11aS)-3,7-Bis[2,4,6-tris(1-methylethyl)phenyl]-10,11,12,13-tetrahydro-5-hydroxy-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin 5-oxide is a chemical compound with a complex and lengthy name. It is a phosphorus-containing compound that contains two phosphorus atoms and a dioxaphosphocin oxide ring system. The compound also contains a diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin ring system. Additionally, it has hydroxyl (OH) and isopropyl (C3H7) groups attached to phenyl rings. The compound's structure and properties make it potentially useful in organic synthesis and as a building block for other chemical compounds.

Upstream product

• 21524-34-5 2,4,6-triisopropyl-1-bromobenzene 
• 1258276-29-7 (R)-6,6'-diiodo-7,7'-bis(methoxymethoxy)-2,2',3,3'-tetrahydro-1,1'-spirobiindane 
• 1258276-31-1 (R)-6,6'-bis(2,4,6-triisopropylphenyl)-1,1'-spirobiindane-7,7'-diol 

Relevant articles and documents

Asymmetric allylboration of aldehydes with pinacol allylboronates catalyzed by 1,1′-spirobiindane-7,7′-diol (SPINOL) based phosphoric acids

The asymmetric allylboration of aldehydes with pinacolallylboronates catalyzed by 1,1′-spirobiindane-7,7′-diol (SPINOL) based phosphoric acids is described. 6,6′-Bis(2,4,6-triisopropylphenyl)SPINOL-based phosphoric acid was found to be a general, highly e