(R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl
Suppliers
Names
[ CAS No. ]:
76189-55-4
[ Name ]:
(R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl
[Synonym ]:
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
Chemical & Physical Properties
[ Boiling Point ]:
724.3±55.0 °C at 760 mmHg
[ 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
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ 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 & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2902909090
[ Summary ]:
2902909090 other aromatic hydrocarbons。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:2.0%。General tariff:30.0%
Articles
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...
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...
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...