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Gadolinium(III) tris(isopropoxide)_Molecular_structure_CAS_14532-05-9)
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Gadolinium(III) tris(isopropoxide)

Catalog No. 663948 Name Sigma Aldrich
CAS Number 14532-05-9 Website http://www.sigmaaldrich.com
M. F. C9H21GdO3 Telephone 1-800-521-8956
M. W. 334.51124 Fax
Purity 99% Email
Storage Chembase ID: 140533

SYNONYMS

Title
三异丙醇钆
IUPAC name
tris(propan-2-yloxy)gadolinium
IUPAC Traditional name
triisopropoxygadolinium
Synonyms
Tris(isopropoxy) gadolinium(III)

DATABASE IDS

CAS Number 14532-05-9
MDL Number MFCD00144381

PROPERTIES

Empirical Formula (Hill Notation) C9H21GdO3
Purity 99%
Melting Point >300 °C
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-37/39
German water hazard class 3

DETAILS

Description (English)
Application
Catalyst used in a ring opening of meso-aziridines with trimethylsilyl azide.5
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.
Catalyst for:
• Enantioselective construction of beta-quaternary carbons via conjugate addition reactions1
• Generation of reactive enolates2
• Regioselective / stereoselective conjugate addition of cyanide to enones3
• Strecker reactions4
• Asymmetric ring-opening of meso-aziridines5
Packaging
3 g in ampule
500 mg in ampule
Description (简体中文)
Application
在很多不对称催化应用中,应当使用手套箱和 Schlenk 技术防止此稀土催化剂与空气和水分接触,因为这两个因素将对反应结果产生不利影响。用无水溶剂配制该催化剂溶液并立即使用。
用三甲基硅叠氮使内消旋-氮杂环丙烷开环的催化剂。5
Catalyst for:
• Enantioselective construction of beta-quaternary carbons via conjugate addition reactions1
• Generation of reactive enolates2
• Regioselective / stereoselective conjugate addition of cyanide to enones3
• Strecker reactions4
• Asymmetric ring-opening of meso-aziridines5
包装
3 g in ampule
500 mg in ampule

REFERENCES