(11bR)-2,6-Di-9-phenanthrenyl-4-hydroxy-dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-oxide
- ₹25601.13
- Product name: (11bR)-2,6-Di-9-phenanthrenyl-4-hydroxy-dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-oxide
- CAS: 864943-22-6
- MF: C48H29O4P
- MW: 700.72
- EINECS:
- MDL Number:MFCD12546016
- Synonyms:(R)-3,3′-Bis(9-phenanthryl)-1,1′-binaphthalene-2,2′-diyl hydrogen phosphate;(11bR)-2,6-Di-9-phenanthrenyl-4-hydroxy-dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-oxide;(11bS)-4-hydroxy-2,6-di(phenanthren-9-yl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide;(11bR)-2,6-Di-9-phenanthrenyl-4-hydroxy-4-oxidedinaphtho[ 2,1-d:1',2'-f][1,3,2]dioxaphosphepin;(11bR)-2,6-Di-9-phenanthrenyl-4-hydroxy-4-oxide,99%e.e.;(R)-3,3'-Bis(9-phenanthrenyl)-1,1'-binaphthyl-2,2'-diyl Hydrogen Phosphate;SF110065;(11bR)-2,6-Di-9-phenanthrenyl-4-hydroxy-dinaphtho[2,1-d
1 prices
Selected condition:
Brand
- Sigma-Aldrich(India)
Package
- 100MG
- ManufacturerSigma-Aldrich(India)
- Product number700665
- Product description(11bR)-2,6-Di-9-phenanthrenyl-4-hydroxy-dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-oxide
- Packaging100MG
- Price₹25601.13
- Updated2022-06-14
- Buy
Manufacturer | Product number | Product description | Packaging | Price | Updated | Buy |
---|---|---|---|---|---|---|
Sigma-Aldrich(India) | 700665 | (11bR)-2,6-Di-9-phenanthrenyl-4-hydroxy-dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-oxide | 100MG | ₹25601.13 | 2022-06-14 | Buy |
Properties
Melting point :390-400°C
Density :1.46±0.1 g/cm3(Predicted)
storage temp. :-20°C
pka :1.11±0.20(Predicted)
optical activity :[α]22/D 44.0°, c = 1 in DMSO
CAS DataBase Reference :864943-22-6
Density :1.46±0.1 g/cm3(Predicted)
storage temp. :-20°C
pka :1.11±0.20(Predicted)
optical activity :[α]22/D 44.0°, c = 1 in DMSO
CAS DataBase Reference :864943-22-6
Safety Information
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Signal word: | Warning | ||||||||||||||
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Description
Catalyst for:- Asymmetric hydrogenation cascade
- Enantioselective Friedel-Crafts reaction
- Asymmetric hydrogenation of 2-substituted quinolines
- Chiral Broensted acid catalyzed enantioselective a-aminoxylation of ene carbamates
- Preparation of β-carbolines via diastereo- and enantioselective N-acyliminium cyclization cascades of tryptamines and keto acids/esters
- Asymmetric transfer hydrogenation of substituted quinoxalines
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