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Merck
CN

663948

三异丙醇钆

99%, solid

别名:

Tris(isopropoxy) gadolinium(III)

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关于此项目

经验公式(希尔记法):
C9H21GdO3
化学文摘社编号:
分子量:
334.51
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.22
MDL number:
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产品名称

三异丙醇钆, 99%

Quality Segment

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

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。
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


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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分析证书(COA)

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相关内容

Shibasaki's research focuses on novel asymmetric catalytic systems for streamlined synthesis of enantioenriched chiral building blocks.


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



全球贸易项目编号

货号GTIN
663948-3G04061833411513
663948-500MG04061833549186