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Sigma-Aldrich

Europium(III) tris[3-(heptafluoropropylhydroxymethylene)-d-camphorate]

puriss. p.a., for NMR spectroscopy

Sinônimo(s):

Eu(hfc)3, Tris[3-(heptafluoropropylhydroxymethylene)-d-camphorato]europium(III)

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About This Item

Fórmula empírica (Notação de Hill):
C42H42EuF21O6
Número CAS:
34788-82-4
Peso molecular:
1193.71
Número CE:
252-214-0
Número MDL:
MFCD00151059
Código UNSPSC:
12352115
ID de substância PubChem:
329770226
NACRES:
NA.22

grau

for NMR spectroscopy
puriss. p.a.

Nível de qualidade

100

forma

powder

pf

~160 °C (lit.)

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

CC1(C)C2CC[C@@]1(C)C(=O)C2=C(O[Eu](OC(=C3C4CC[C@@](C)(C3=O)C4(C)C)C(F)(F)C(F)(F)C(F)(F)F)OC(=C5C6CC[C@@](C)(C5=O)C6(C)C)C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/3C14H15F7O2.Eu/c3*1-10(2)6-4-5-11(10,3)8(22)7(6)9(23)12(15,16)13(17,18)14(19,20)21;/h3*6,23H,4-5H2,1-3H3;/q;;;+3/p-3/b3*9-7+;/t3*6-,11+;/m111./s1

chave InChI

VGLKHVQPWGFXEG-PSMAIOHISA-K

Categorias relacionadas

Aplicação

It may be used as the NMR shift reagent in the 1H NMR analysis to determine the following:
  • Enantiomeric purities of the precursors of trisporic acids A, B and related products.
  • Optical purity of racemic 6,7-dichloro-5-methoxy-2-methyl-2-phenyl-1 indanone.
  • Epimeric purity of 4-methylsulfinylbutylglucosinolate.

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Outras notas

Chiral shift reagent for the determination of enantiomer ratios by NMR ; Measurements in polar solvents; For use as a Lanthanide shift reagent

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number
BCCH2268
BCCD8638
BCCC8416
BCBZ2683
BCBV1108

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M. Calmes et al.
Tetrahedron, 43, 2285-2285 (1987)
Pirkle et al.
The Journal of Organic Chemistry, 44, 1025-1025 (1979)
Optical purity determination and 1H-NMR spectral simplification with lanthanide shift reagents-VIII. An indacrinone precursor, 6, 7-dichloro-5-methoxy-2-methyl-2-phenyl-1-indanone.
Hatzis A and Rothchild R.
Journal of Pharmaceutical and Biomedical Analysis, 4(4), 443-449 (1986)
Enantioselective synthesis of the white key intermediate for the synthesis of trisporic acids.
Bacigaluppo JA, et al.
Tetrahedron Asymmetry, 5(10), 1877-1880 (1994)
Determination of the absolute configuration of the glucosinolate methyl sulfoxide group reveals a stereospecific biosynthesis of the side chain.
Vergara F, et al.
Phytochemistry, 69(15), 2737-2742 (2008)
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