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(bis(N-methylimidazol-2-yl)ethane)dicarbonyliridium(I) tetraphenylborate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

949164-70-9

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949164-70-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 949164-70-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,9,1,6 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 949164-70:
(8*9)+(7*4)+(6*9)+(5*1)+(4*6)+(3*4)+(2*7)+(1*0)=209
209 % 10 = 9
So 949164-70-9 is a valid CAS Registry Number.

949164-70-9Downstream Products

949164-70-9Relevant academic research and scientific papers

Late transition metal catalyzed intramolecular hydroamination: The effect of ligand and substrate structure

Burling, Suzanne,Field, Leslie D.,Messerle, Barbara A.,Rumble, Sarah L.

, p. 4335 - 4343 (2008/10/09)

A series of cationic rhodium(I) and iridium(I) complexes of the type [M(N-N)(CO)2][BPh4 containing the imidazole-based bidentate nitrogen donor ligands (N-N), including bis(N-methylimidazol-2-yl) methane (bim) (1, a M = Rh, b M = Ir), bis(N-methylimidazol-2-yl)ketone (bik) (5, a M = Rh, b M = Ir), 1,1-bis(N-methylimidazol-2-yl)ethane (bie) (3, M = Rh), 2,2-bis(N-methylimidazol-2-yl)propane (bip) (4, M = Rh), and bis(N-methylbenzimidazol-2-yl)methane (bbnzim) (6a M = Rh, 6b M = Ir), were synthesized and characterized. Complexes incorporating the pyrazole analogue bis(1-pyrazolyl)methane (bpm) [M(bpm)(CO)2] [BPh4] (2, a M = Rh, b M = Ir) were also prepared. The efficiency of each of the complexes as catalysts for the cyclization of 4-pentyn-1-amine to 2-methyl-1-pyrroline is reported. The influence of structural variations of the nitrogen donor ligand on the catalytic efficiency of cationic complexes of the type [M(N-N)(CO) 2][BPh4] for the hydroamination reaction was found to be much less than the influence of the nature of the counterion. The scope of the substrates for the intramolecular hydroamination of alkynamines was also investigated using Rh and Ir catalysts with the bim and bpm ligands, using 3-butyn-1-amine (7a), 3-pentyn-1-amine (7b), 4-phenyl-3-butyn-1-amine (7c), 4-pentyn-1-amine (8a), 4-hexyn-1-amine (8b), 5-phenyl-4-pentyn-l-amine (8c), 5-hexyn-1-amine (9), and 6-heptyn-1-amine (10) as substrates. The rhodium and iridium catalysts under investigation preferentially catalyze the formation of five-membered rings and do not catalyze the formation of four- or seven-membered rings. The effect of the substituents on the alkyne on the efficiency of hydroamination differentiates Rh(I) and Ir(I) and suggests the nature of the reactive metal-bound alkynyl intermediate.

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