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(R)-(6,6′-Dimethoxybiphenyl-2,2′-diyl)bis[bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphine]_Molecular_structure_CAS_352655-61-9)
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(R)-(6,6′-Dimethoxybiphenyl-2,2′-diyl)bis[bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphine]

Catalog No. 29512 Name Sigma Aldrich
CAS Number 352655-61-9 Website http://www.sigmaaldrich.com
M. F. C74H104O6P2 Telephone 1-800-521-8956
M. W. 1151.561482 Fax
Purity ≥97% Email
Storage Chembase ID: 141349

SYNONYMS

Title
(R)-(6,6′-二甲氧基联苯-2,2′-二基)二[双(3,5-二-叔丁基-4-甲氧苯基)膦]
IUPAC name
(2-{2-[bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphanyl]-6-methoxyphenyl}-3-methoxyphenyl)bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphane
IUPAC Traditional name
(2-{2-[bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphanyl]-6-methoxyphenyl}-3-methoxyphenyl)bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphane
Synonyms
(R)-3,5-t-Bu-4-MeO-MeOBIPHEP
(R)-[6,6′-二甲氧基(1,1′-联苯基)-2,2′-二基]二{双[3,5-二(1,1-二甲基乙基)-4-甲氧苯基]膦}
SL-A109-1
(R)-[6,6′-Dimethoxy(1,1′-biphenyl)-2,2′-diyl]bis{bis[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]phosphine}

DATABASE IDS

MDL Number MFCD09265029
CAS Number 352655-61-9

PROPERTIES

Empirical Formula (Hill Notation) C74H104O6P2
Optical Purity ee: ≥99%
Purity ≥97%
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (English)
General description
sold in collaboration with Solvias AG
Packaging
1, 5 g in glass bottle
100, 500 mg in glass bottle
Application
Atropisomeric MeOBIPHEP ligands
• Asymmetrical conjugate addition of arylboronic acids to maleimides and enones catalyzed by rhodium complexes1
• Intramolecular ketone hydroacylation2
• Desymmetrization through enantioselective C-C bond activation and ring expansion of allenyl cyclobutanols3
• Hydroamination of bicyclic alkenes and dienes with anilines4
• 1,4-addition/asymmetric protonation of amino acrylates5
Description (简体中文)
General description
与 Solvias AG 联合销售
包装
1, 5 g in glass bottle
100, 500 mg in glass bottle
Application
Atropisomeric MeOBIPHEP ligands
• Asymmetrical conjugate addition of arylboronic acids to maleimides and enones catalyzed by rhodium complexes1
• Intramolecular ketone hydroacylation2
• Desymmetrization through enantioselective C-C bond activation and ring expansion of allenyl cyclobutanols3
• Hydroamination of bicyclic alkenes and dienes with anilines4
• 1,4-addition/asymmetric protonation of amino acrylates5

REFERENCES