(S)-(-)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl

Modify Date: 2024-01-11 10:50:50

(S)-(-)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl Structure
(S)-(-)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl structure
Common Name (S)-(-)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl
CAS Number 76189-56-5 Molecular Weight 622.67
Density N/A Boiling Point 724.3±55.0 °C at 760 mmHg
Molecular Formula C44H32P2 Melting Point 239-242ºC
MSDS Chinese USA Flash Point 419.0±37.8 °C

 Use of (S)-(-)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl


(S)-BINAP is the inactive isomer of (R)-BINAP (HY-W017757), and can be used as an experimental control. (R)-BINAP is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name (S)-(-)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl
Synonym More Synonyms

  Biological Activity

Description (S)-BINAP is the inactive isomer of (R)-BINAP (HY-W017757), and can be used as an experimental control. (R)-BINAP is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog
References

[1]. Nathalia Azevedo Portilho, et al. The DNMT1 inhibitor GSK-3484862 mediates global demethylation in murine embryonic stem cells.

[2]. Keystone Symposia 2019 - Epigenetics and Human Disease

 Chemical & Physical Properties

Boiling Point 724.3±55.0 °C at 760 mmHg
Melting Point 239-242ºC
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)

 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 S26-S37/39
RIDADR NONH for all modes of transport
WGK Germany 3

 Articles11

More Articles
On the mechanism of an asymmetric alpha,beta-unsaturated carboxylic acid hydrogenation: application to the synthesis of a PGD2 receptor antagonist.

J. Am. Chem. Soc. 128 , 17063, (2006)

Ruthenium complexes employing axially chiral ligands were found to be effective asymmetric hydrogenation catalysts for the reduction of alpha,beta-unsaturated ene acid 1-E to give 2, a prostaglandin D...

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...

Ohkuma, T. et al.

J. Am. Chem. Soc. 117 , 2675, (1995)

 Synonyms

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)
rac-binap
UNII:OX12238KWH
(r)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl
BINAP
[1,1'-Binaphthalene]-2,2'-diylbis[diphenylphosphine]
MFCD00010805
UNII:970O8508MB
UNII:4F1X2F8NA3
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