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Merck
CN

669873

(Λ,R)-BINPHAT tetrabutylammonium salt

≥95.0% (31P-NMR)

Synonym(s):

[Tetrabutylammonium][(Λ,R)-(1,1′-binaphthalene-2,2′diolato)(bis(tetrachlor-1,2-benzenediolato)phosphat(V))]

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About This Item

Empirical Formula (Hill Notation):
C32H12Cl8O6P · C16H36N
Molecular Weight:
1049.50
UNSPSC Code:
12352000
PubChem Substance ID:
MDL number:
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InChI

1S/C32H12Cl8O6P.C16H36N/c33-21-22(34)26(38)30-29(25(21)37)43-47(44-30,45-31-27(39)23(35)24(36)28(40)32(31)46-47)41-17-11-9-13-5-1-3-7-15(13)19(17)20-16-8-4-2-6-14(16)10-12-18(20)42-47;1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4/h1-12H;5-16H2,1-4H3/q-1;+1

SMILES string

CCCC[N+](CCCC)(CCCC)CCCC.Clc1c(Cl)c(Cl)c2O[P-]34(Oc5ccc6ccccc6c5-c7c(O3)ccc8ccccc78)(Oc2c1Cl)Oc9c(Cl)c(Cl)c(Cl)c(Cl)c9O4

InChI key

YJHXQLMGOKCETI-UHFFFAOYSA-N

assay

≥95.0% (31P-NMR)

impurities

≤5.0% Δ-TRISPHAT tetrabutylammonium salt

storage temp.

2-8°C

Application

Chiral anion mediated asymmetric chemistry

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Jerome Lacour et al.
Organic & biomolecular chemistry, 3(1), 15-19 (2004-12-17)
Chemical reactions and processes often involve chiral, yet racemic, cationic reagents, intermediates or products. To afford instead non racemic or enantiopure compounds, an asymmetric ion pairing of the cations with enantiopure anions can be considered--the counter ions behaving as asymmetric
Jérôme Lacour et al.
Chemical Society reviews, 32(6), 373-382 (2003-12-16)
Chemical reactions and processes often involve cationic prostereogenic or racemic reagents, intermediates or products. To afford instead non-racemic or enantiopure compounds, an asymmetric ion pairing of the cations with chiral anionic counterions can be considered. This review presents recent examples
Chiral ion mediated asym. chemistry
Lacour, J.
Chimia, 56, 672-675 (2002)

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