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About This Item
Empirical Formula (Hill Notation):
C9H21LaO3
CAS Number:
Molecular Weight:
316.17
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22
MDL number:
Product Name
Lanthanum(III) isopropoxide, 98%
Quality Level
assay
98%
form
solid
reaction suitability
core: lanthanum, reagent type: catalyst
SMILES string
CC(C)O[La](OC(C)C)OC(C)C
InChI
1S/3C3H7O.La/c3*1-3(2)4;/h3*3H,1-2H3;/q3*-1;+3
InChI key
SORGMJIXNUWMMR-UHFFFAOYSA-N
Application
Complex with an (S,S)-phenyl-linked-binaphthol which promotes a catalytic 1,4-addition of malonate to cyclic and acyclic enones. Co-catalyst with CuF-triphenylphosphine in a general catalytic allylation of ketoimines.
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.
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
4.1B - Flammable solid hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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Related Content
Shibasaki's research focuses on novel asymmetric catalytic systems for streamlined synthesis of enantioenriched chiral building blocks.
Tetrahedron Letters, 48, 2815-2815 (2007)
Reiko Wada et al.
Journal of the American Chemical Society, 128(23), 7687-7691 (2006-06-08)
A general catalytic allylation of simple ketoimines was developed using 1 mol % of CuF.3PPh(3) as catalyst, 1.5 mol % of La(O(i)Pr)(3) as the cocatalyst, and stable and nontoxic allylboronic acid pinacol ester as the nucleophile. This reaction constituted a
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 665193-500MG | 04061833549254 |
| 665193-3G | 04061833549247 |

