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(11bS,11′bS)-4,4′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis-dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin_Molecular_structure_CAS_349114-57-4)
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(11bS,11′bS)-4,4′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis-dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin

Catalog No. 682869 Name Sigma Aldrich
CAS Number 349114-57-4 Website http://www.sigmaaldrich.com
M. F. C55H76O5P2 Telephone 1-800-521-8956
M. W. 879.136462 Fax
Purity Email
Storage Chembase ID: 141453

SYNONYMS

Title
(11bS,11′bS)-4,4′-(9,9-二甲基-9H-氧杂蒽-4,5-二基)双-二萘并[2,1-d:1′,2′-f][1,3,2]二噁磷杂庚英
IUPAC name
13-(5-{12,14-dioxa-13-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosan-13-yl}-9,9-dimethyl-9H-xanthen-4-yl)-12,14-dioxa-13-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosane
IUPAC Traditional name
13-(5-{12,14-dioxa-13-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosan-13-yl}-9,9-dimethylxanthen-4-yl)-12,14-dioxa-13-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosane
Synonyms
S,S-Reetz X-Diphosphonite
S,S-Reetz X-二亚磷酸酯

DATABASE IDS

CAS Number 349114-57-4
MDL Number MFCD09842740

PROPERTIES

Empirical Formula (Hill Notation) C55H36O5P2
Melting Point 195-207 °C (dec.)
Optical Rotation [α]22/D -245°, c = 1 in chloroform
MSDS Link Download
German water hazard class 3

DETAILS

Description (English)
Application
This diphosphonite ligand has been successfully employed in Noyori-type asymmetric transfer hydrogenation of prochiral ketones.3

• Catalyst for asymmetric hydrogenation of quinolines catalyzed by iridium complexes of BINOL-derived diphosphonites1
• Ligand in asymmetric Ni-catalyzed hydrocyanation of styrene and other vinylarenes2
Packaging
100, 500 mg in glass bottle
Description (简体中文)
Application
这种二亚磷酸酯配体已成功应用于前手性酮的 Noyori 型不对称转移氢化反应。3

• Catalyst for asymmetric hydrogenation of quinolines catalyzed by iridium complexes of BINOL-derived diphosphonites1
• Ligand in asymmetric Ni-catalyzed hydrocyanation of styrene and other vinylarenes2
包装
100, 500 mg in glass bottle

REFERENCES