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Merck
CN

440590

(R)-(−)-1,1′-Bi-2-naphthol bis(trifluoromethanesulfonate)

97%

Synonym(s):

(R)-1,1′-Bi(2-naphthol) bis(trifluoromethanesulfonate), (R)-1,1′-Binaphthalene-2,2′-diyl bis(trifluoromethanesulfonate)

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About This Item

Linear Formula:
(CF3SO3C10H6-)2
CAS Number:
126613-06-7
Molecular Weight:
550.45
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
24867612
MDL number:
MFCD00274615
Beilstein/REAXYS Number:
4282753

Key Documents

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Product Name

(R)-(−)-1,1′-Bi-2-naphthol bis(trifluoromethanesulfonate), 97%

InChI

1S/C22H12F6O6S2/c23-21(24,25)35(29,30)33-17-11-9-13-5-1-3-7-15(13)19(17)20-16-8-4-2-6-14(16)10-12-18(20)34-36(31,32)22(26,27)28/h1-12H

SMILES string

FC(F)(F)S(=O)(=O)Oc1ccc2ccccc2c1-c3c(OS(=O)(=O)C(F)(F)F)ccc4ccccc34

InChI key

OYJLCOSEYYZULE-UHFFFAOYSA-N

assay

97%

optical activity

[α]23/D −146°, c = 1 in chloroform

mp

82-85 °C (lit.)

Application

(R)-(−)-1,1′-Bi-2-naphthol bis(trifluoromethanesulfonate) can be used:
  • In the synthesis of heterobidentate ligands for asymmetric catalysis.
  • To prepare 2-(diphenylphosphino)-2′-alkoxy-1,1′-binaphthyls by reacting with bis(aryl) phosphonic acids.
  • As a starting material for the synthesis of binaphthyl based rhodium catalysts used in the hydrogenation of styrene.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
07906BQ
00411TI
16413ER

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Novel heterobidentate ligands for asymmetric catalysis: Synthesis and rhodium-catalysed reactions of S-alkyl (R)-2-diphenylphosphino-1, 1′-binaphthyl-2′-thiol
Gladiali S, et al.
Tetrahedron Asymmetry, 5(7), 1143-1146 (1994)
New perfluorinated rhodium-BINAP catalysts and hydrogenation of styrene in supercritical CO2
Altinel H, et al.
Journal of Supercritical Fluids, 51(2), 202-208 (2009)
Synthesis of chiral 2, 2′-bis (diphenylphosphino)-1, 1′-binaphthyl (BINAP) via a novel nickel-catalyzed phosphine insertion
Cai D, et al.
The Journal of Organic Chemistry, 59(23), 7180-7181 (1994)
Palladium-catalysed asymmetric allylic alkylation in the presence of a chiral `light fluorous? phosphine ligand
Cavazzini M, et al.
Chemical Communications (Cambridge, England), 13, 1220-1221 (2001)

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