Company Name: |
Shanghai Anyinuo Biomedical Technology Co., Ltd. Gold
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Tel: |
021-34625901 |
Email: |
420970979@qq.com |
Products Intro: |
Product Name:(R)-(5,5'-Dichloro-6,6'-dimethoxy-[1,1'-biphenyl]-2,2'-diyl)bis(diphenylphosphine) CAS:185913-97-7 Purity:>=98% Package:100mg;250mg;500mg;1g;10g;100g;1kg
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Company Name: |
J & K SCIENTIFIC LTD.
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Tel: |
010-82848833 400-666-7788 |
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jkinfo@jkchemical.com |
Products Intro: |
Product Name:(R)-(+)-5,5'-Dichloro-6,6'-dimethoxy-2,2'-bis(diphenylphosphino)-1,1'-biphenyl, min. 95% (R)-Cl-MeO-BIPHEP CAS:185913-97-7 Purity:min. 95% Package:1g;250mg
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| (R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL Basic information | Description |
Product Name: | (R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL | Synonyms: | (R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL;(R)-CL-MEO-BIPHEP;(S)-(-)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL;(S)-CL-MEO-BIPHEP;(-)-2,2'-BIS(DIPHENYLPHOSPHINO)-5,5'-DICHLORO-6,6'-DIMETHOXY-1,1'-BIPHENYL;(+)-2,2'-BIS(DIPHENYLPHOSPHINO)-5,5'-DICHLORO-6,6'-DIMETHOXY-1,1'-BIPHENYL;(-)-5,5'-DICHLORO-2,2'-BIS(DIPHENYLPHOSPHINO)-6,6'-DIMETHOXY-1,1'-BIPHENYL;(+)-5,5'-DICHLORO-2,2'-BIS(DIPHENYLPHOSPHINO)-6,6'-DIMETHOXY-1,1'-BIPHENYL | CAS: | 185913-97-7 | MF: | C38H30Cl2O2P2 | MW: | 651.5 | EINECS: | | Product Categories: | Chiral Phosphine;MeOBIPHEP Series | Mol File: | 185913-97-7.mol | |
| (R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL Chemical Properties |
Melting point | 176-180 °C | Boiling point | 678.2±55.0 °C(Predicted) | form | Powder | color | yellow-white | optical activity | [α]/D +59±4°, c = 1% in chloroform |
| (R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL Usage And Synthesis |
Description | 1. Ligand used in the ruthenium catalyzed, enantioselective hydrogenation of alkenes, carbonyls, and imines. 2. Ligand used in the rhodium-catalyzed cyclization of acetylenic aldehydes. 3. Ligand used in the iridium-catalyzed hydrogenative coupling of alkynes to aromatic and aliphatic N-arylsulfonyl aldimines. 4. Asymmetric Cu-catalyzed propargylic substitution with amines,4a and enamines.4b 5. Catalytic desymmetrizing intramolecular Heck reaction. 6. Assembly of 1,3-polyols. 7. Pd-catalyzed diastereo/enantioselective allylic alkylations of ketone enolates. 8. Enantioselective vinylogous Reformatsky-type addition. 9. Cu-catalyzed chemoselective preparation of 2-(pinacolato)boron- substituted allylcopper complexes. and their In situ site-, diastereo-, and enantioselective additions to ketones.
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| (R)-(+)-5,5'-DICHLORO-6,6'-DIMETHOXY-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BIPHENYL Preparation Products And Raw materials |
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