Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

663948

Sigma-Aldrich

Gadolinium(III) tris(isopropoxide)

99%

Synonym(s):

Tris(isopropoxy) gadolinium(III)

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C9H21GdO3
CAS Number:
Molecular Weight:
334.51
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

form

solid

reaction suitability

core: gadolinium
reagent type: catalyst

mp

>300 °C

SMILES string

CC(C)O[Gd](OC(C)C)OC(C)C

InChI

1S/3C3H7O.Gd/c3*1-3(2)4;/h3*3H,1-2H3;/q3*-1;+3

InChI key

VJLSFXQJAXVOEQ-UHFFFAOYSA-N

Application

Catalyst for:
  • Enantioselective construction of beta-quaternary carbons via conjugate addition reactions
  • Generation of reactive enolates
  • Regioselective / stereoselective conjugate addition of cyanide to enones
  • Strecker reactions
  • Asymmetric ring-opening of meso-aziridines
Catalyst used in a ring opening of meso-aziridines with trimethylsilyl azide.
In many asymmetric catalysis applications, glove box and Schlenk techniques should be employed to prevent exposure of the rare earth catalyst to air and moisture, which can be detrimental to the reaction outcome. Solutions of the catalyst should be made using anhydrous solvents and used shortly after preparation.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Yuhei Fukuta et al.
Journal of the American Chemical Society, 128(19), 6312-6313 (2006-05-11)
An asymmetric ring-opening reaction of meso-aziridines with TMSN3 was developed using a catalyst prepared from Y(OiPr)3 and chiral ligand 2 in a 1:2 ratio. Excellent enantioselectivity was realized from a wide range of substrates with a practical catalyst loading. The

Related Content

Professor Shibasaki's research focuses on the development of novel cooperative asymmetric catalytic systems that allowed for streamlined synthesis of enantioenriched high-value chiral building blocks.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service