(S,S)-F-BINAPHANE

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Company Name: BOC Sciences
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Products Intro: Product Name:1,1'-Bis{(S)-4,5-dihydro-3H-binaphtho[1,2-c:2',1'-e]phosphino}ferrocene
CAS:544461-38-3
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Products Intro: Product Name:1,1'-Bis{(S)-4,5-dihydro-3H-binaphtho[1,2-c:2',1'-e]phosphino}ferrocene
CAS:544461-38-3
Purity:98% Package:$128.9/100mg;Bulk package Remarks:98%
Company Name: J & K SCIENTIFIC LTD.  
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Products Intro: Product Name:1,1'-Bis{(S)-4,5-dihydro-3H-binaphtho[1,2-c:2',1'-e]phosphino}ferrocene, min. 98% (S,S)-f-Binaphane
CAS:544461-38-3
Purity:min. 98% Package:100mg;500mg
Company Name: Shanghai Aladdin Bio-Chem Technology Co.,LTD  
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Products Intro: Product Name:1,1'-Bis{(S)-4,5-dihydro-3H-binaphtho[1,2-c:2',1'-e]phosphino}ferrocene
CAS:544461-38-3
Purity:≥98% Package:25mg/RMB 774.90;100mg/RMB 2476.90
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
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Products Intro: Product Name:(S,S)-F-BINAPHANE
CAS:544461-38-3
Purity:98% Package:100mg Remarks:S53356
(S,S)-F-BINAPHANE Basic information
Reaction
Product Name:(S,S)-F-BINAPHANE
Synonyms:(S,S)-F-BINAPHANE;1,1'-Bis{(S)-4,5-dihydro-3H-binaphtho[1,2-c:2',1'-e]phosphino}ferrocene, Min. 98% (S,S)-f-Binaphane;1,1μ-Bis[(S)-4,5-dihydro-3H-binaphtho[2,1-c:1μ,2μ-e]phosphepino]ferrocene, 1,1μ-Bis[(11bs)-3,5-dihydro-4H-dinaphtho[2,1-c:1μ,2μ-e]phosphenpin-4yl]ferrocene;1,1'-Bis[(S)-4,5-dihydro-3H-binaphtho[1,2-c:2',1'-e]phosphino]ferrocene;1,1'-Bis{(S)-4,5-dihydro-3H-binaphtho[1,2-c:2',1'-e]phosphino}ferrocene (S,S)-f-Binaphane;1,1'-Bis{(S)-4,5-dihydro-3H-binaphtho[1,2-c:2',1'-e]phosphino}ferrocene
CAS:544461-38-3
MF:C54H32FeP2
MW:798.64
EINECS:
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Mol File:544461-38-3.mol
(S,S)-F-BINAPHANE Structure
(S,S)-F-BINAPHANE Chemical Properties
storage temp. 2-8°C, protect from light, stored under nitrogen
form Powder
color yellow-brown
Sensitive air sensitive, light sensitive
Safety Information
MSDS Information
(S,S)-F-BINAPHANE Usage And Synthesis
Reaction
  1. Ligand for enantioselective Pd-catalyzed hydrogenation of enesulfonamides [5] and cyclic Nsulfonylimines.
  2. Enantioselective, asymmetric organocatalyst for cycloaddition of allenoates to C60 fullerene (conversion >90%, ee up to 90%)
  3. Ligand for Iridium-mediated direct asymmetric reductive amination of acetophenone with phenylhydrazide (conversion >99%; yield >94%; ee >94%)
  4. Ligand used for the palladium-catalyzed, asymmetric, decarboxylative generation and asymmetric allylation of α-imino anions.
  5. Ligand used in iridium-catalyzed, asymmetric hydrogenation of 6-substituted 3-hydroxypyridinium salts to trans 6-substituted piperidin-3-ols with high enantioselectivities(up to 95% ee).
Reactions of 544461-38-3_1
Reactions of 544461-38-3_2
(S,S)-F-BINAPHANE Preparation Products And Raw materials
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(S,S)-F-BINAPHANE