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(OCMeCHCMeN(2,6-(i)Pr2C6H3))AlCl2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

478967-92-9

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478967-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 478967-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,9,6 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 478967-92:
(8*4)+(7*7)+(6*8)+(5*9)+(4*6)+(3*7)+(2*9)+(1*2)=239
239 % 10 = 9
So 478967-92-9 is a valid CAS Registry Number.

478967-92-9Downstream Products

478967-92-9Relevant academic research and scientific papers

Four- and five-coordinate aluminum ketiminate complexes: Synthesis, characterization, and ring-opening polymerization

Yu, Ru-Ching,Hung, Chen-Hsiung,Huang, Jui-Hsien,Lee, Horng-Yi,Chen, Jwu-Ting

, p. 6450 - 6455 (2008/10/08)

A series of aluminum complexes featuring with the ketiminate ligand, OCMeCHCMeNHAr (Ar = 2,6-iPr2C6H3, 1), have been prepared and characterized spectroscopically and structurally. Reactions of 1 with trialkylaluminum in 1:1 or 1:2 molar ratio generate four- and five-coordinated aluminum complexes (OCMeCHCMeNAr)AlR2 (R = Me (2); R = Et (3)) and (OCMeCHCMeNAr)2AlR (R = Me (4); R = Et (5)) in high yields. Similarly, reaction of AlCl3 with 1 or 2 equiv of the lithiated 1 in toluene afforded bis(ketiminate) aluminum chloride complex, (OCMeCHCMeNAr)2AlCl (6) or (OCMeCHCMeNAr)AlCl2 (7). Surprisingly, reacting 6 with 1 equiv of AgBF4 in methylene/acetonitrile mixsolvents generates (OCMeCHCMeNAr)2AlF (8) in moderate yield. The structures of complexes 2-6 and 8 have been determined by X-ray crystallography. Complexes 2 and 3 both exhibit tetrahedron structures with the aluminum atom surrounded by oxygen and nitrogen atoms of chelating ketiminate and two alkyl groups. The mono- and bis-ketiminate aluminum complexes 2 - 5 have shown moderate activity toward the ring-opening polymerization of ε-caprolactone.

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