(R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl structure
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Common Name | (R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl | ||
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CAS Number | 76189-55-4 | Molecular Weight | 622.67 | |
Density | N/A | Boiling Point | 724.3±55.0 °C at 760 mmHg | |
Molecular Formula | C44H32P2 | Melting Point | 283-286 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 419.0±37.8 °C |
Use of (R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl(R)-BINAP is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | (R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl |
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Synonym | More Synonyms |
Description | (R)-BINAP is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog | |
In Vitro | (R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthy 用作金属介导的不对称催化的手性配体。 |
Boiling Point | 724.3±55.0 °C at 760 mmHg |
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Melting Point | 283-286 °C(lit.) |
Molecular Formula | C44H32P2 |
Molecular Weight | 622.67 |
Flash Point | 419.0±37.8 °C |
Exact Mass | 622.197937 |
PSA | 27.18000 |
LogP | 13.38 |
Vapour Pressure | 0.0±2.3 mmHg at 25°C |
Index of Refraction | 235 ° (C=0.3, Toluene) |
Water Solubility | insoluble |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi:Irritant |
Risk Phrases | R36/37/38 |
Safety Phrases | S22-S24/25-S37/39-S26 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2902909090 |
Precursor 0 | |
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DownStream 2 | |
HS Code | 2902909090 |
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Summary | 2902909090 other aromatic hydrocarbons。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:2.0%。General tariff:30.0% |
The preparation of bi-functional organophosphine oxides as potential antitumor agents.
Eur. J. Med. Chem. 45 , 5527-30, (2010) Following our previously reported pyridinyl phosphine oxides as antitumor agents, we targeted the commercially available C(2)-axial chiral organophosphine ligand catalysts, such as 2,2'-bis(diphenylph... |
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Desymmetrization of meso-dienyne by asymmetric Pauson-Khand type reaction catalysts.
Chem. Commun. (Camb.) , 1134-1135, (2004) Desymmetrization of the meso dienynes, such as propargyl 1-vinylallyl N-tosylamides (1a-c) and propargyl 1-vinylallyl ethers (1d-e), by asymmetric Pauson-Khand type reaction catalysts was studied. The... |
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Catalytic enantioselective hetero-Diels-Alder reactions of an azo compound.
J. Am. Chem. Soc. 128 , 16482, (2006) This communication describes studies in which an azo hetero-Diels-Alder adduct was furnished in high regio- and enantioselectivity using azopyridine as a reagent and silver as a catalyst. The obtained... |
2,2'-Bis(diphenylphosphanyl)-1,1'-binaphthalene |
Phosphine, 1,1'-[1,1'-binaphthalene]-2,2'-diylbis[1,1-diphenyl- |
rac-2,2'-Bis-(diphenylphosphino)-1,1'-binaphthyl |
1,1'-binaphthalene-2,2'-diylbis(diphenylphosphane) |
(±)-BINAP |
1,1'-Binaphthalen-2,2'-diylbis(diphenylphosphan) |
1,1'-Binaphthalene-2,2'-diylbis(diphenylphosphine) |
UNII:OX12238KWH |
(r)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl |
BINAP |
[1,1'-Binaphthalene]-2,2'-diylbis[diphenylphosphine] |
MFCD00010805 |
UNII:970O8508MB |
UNII:4F1X2F8NA3 |