1372719-95-3

Basic information

• Product Name: (11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-bis[2,4,6-tris(1-methylethyl)phenyl]-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin 5-oxide
• Synonyms: (11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-bis[2,4,6-tris(1-methylethyl)phenyl]-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin 5-oxide;(11aR)-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;(11aR)-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;(11aR)-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.;Diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin, 10,11,12,13-tetrahydro-5-hydroxy-3,7-bis[2,4,6-tris(1-methylethyl)phenyl]-, 5-oxide, (11aR)-
• CAS NO: 1372719-95-3
• Molecular Formula: C₄₇H₅₉O₄P
• Molecular Weight: 732.926241
• Mol File: 1372719-95-3.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: (11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-bis[2,4,6-tris(1-methylethyl)phenyl]-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin 5-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: (11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-bis[2,4,6-tris(1-methylethyl)phenyl]-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin 5-oxide(1372719-95-3)
• EPA Substance Registry System: (11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-bis[2,4,6-tris(1-methylethyl)phenyl]-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin 5-oxide(1372719-95-3)

Safety Data

• Hazardous Substances Data: 1372719-95-3(Hazardous Substances Data)

Usage

General Description

The chemical "(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-bis[2,4,6-tris(1-methylethyl)phenyl]-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin 5-oxide" is a complex organic compound with a phosphorus-containing ring structure. It is derived from the diindeno-fused dioxaphosphocin, and contains multiple hydroxyl groups and isopropyl-substituted phenyl rings. This chemical compound is likely to have applications in pharmaceutical and materials science, due to its unique structure and potential reactivity. However, given its complexity and novelty, further research and analysis is necessary to fully understand its properties and potential uses.

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