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(scandium)[N(SiMe2(2-methylfuryl))](O-2,6-tBu2C6H3)2)2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1226953-66-7

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1226953-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1226953-66-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,6,9,5 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1226953-66:
(9*1)+(8*2)+(7*2)+(6*6)+(5*9)+(4*5)+(3*3)+(2*6)+(1*6)=167
167 % 10 = 7
So 1226953-66-7 is a valid CAS Registry Number.

1226953-66-7Downstream Products

1226953-66-7Relevant academic research and scientific papers

Group 3 complexes incorporating (furyl)-substituted disilazide ligands

Evans, Lloyd T.J.,Coles, Martyn P.,Cloke, F. Geoffrey N.,Hitchcock, Peter B.

, p. 1114 - 1125 (2010)

A series of mono- and bis-amide scandium and yttrium compounds incorporating the furyl-substituted disilazide ligand, [N{SiMe2R}2]- {i} (where R = 2-methylfuryl) have been synthesized. The compounds Sc{i}Cl2 (1), Sc{i}(CH2SiMe3)2 (2) and Sc{i}(OAr)2 (3) were made from suitable scandium starting materials employing either a salt metathesis protocol with Li{i} or via protonolysis of Sc-C bonds by the neutral amine H{i}. The thermally unstable bis-alkyl yttrium compound, 'Y{i}(CH2SiMe3)2' was isolated as the bis-THF adduct (4) and the bis-aryloxide Y{i}(OAr)2 (5) was synthesized by elimination of LiOAr from Y(OAr)3. The bis-amide complex Y{i}2Cl (6) and conversion to a rare example of an yttrium benzyl compound Y{i}2(CH2Ph) (7) are described. The yttrium cation, [Y{i}2]+, was synthesized by benzyl abstraction from 7 using B(C6F5)3. Structural characterization of representative examples show variation in the coordination modes for amide ligand {i}, differing primarily in the number of furyl groups that coordinate to the metal, with examples in which zero, one or two M-Ofuryl bonds are present. Preliminary investigation in two areas of catalysis are presented.

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