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(1R,2S)-2-N-Methyl-N-(diphenylphosphino)-2-amino-1-phenyl-1-(diphenylphosphinoxy)propane is a complex organic compound with the molecular formula C29H30NP2O. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific (1R,2S) configuration. (1R,2S)-2-N-Methyl-N-(diphenylphosphino)-2-amino-1-phenyl-1-(diphenylphosphinoxy)propane features a central propane chain with a nitrogen atom at the second position, which is substituted with a methyl group and a diphenylphosphino group. The first position of the propane chain is occupied by a phenyl group, and the third position is a phosphinoxy group, also attached to a phenyl ring. This molecule is of interest in the field of organophosphorus chemistry and may have potential applications in catalysis and as a ligand in coordination chemistry due to its unique structure and the presence of both amine and phosphine functionalities.

90032-60-3

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90032-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90032-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,3 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90032-60:
(7*9)+(6*0)+(5*0)+(4*3)+(3*2)+(2*6)+(1*0)=93
93 % 10 = 3
So 90032-60-3 is a valid CAS Registry Number.

90032-60-3Downstream Products

90032-60-3Relevant academic research and scientific papers

Chiral aminophosphine phosphinite-palladium catalysts in asymmetric allylic alkylations

Gong, Liuzhu,Chen, Guoshu,Mi, Aiqiao,Jiang, Yaozhong,Fu, Fangmin,Cui, Xin,Chan, Albert S.C.

, p. 4297 - 4302 (2000)

Palladium complexes of chiral aminophosphine phosphinites were investigated for the asymmetric allylic alkylation of 1,3-diphenyl-2-propenyl acetate with dimethyl malonate. The chirality of the carbon bonded to O-PPh2 in the ligands was found t

Application of P-stereogenic aminophosphine phosphinite ligands in asymmetric hydroformylation

Ewalds, Regine,Eggeling, Eva B.,Hewat, Alison C.,Kamer, Paul C. J.,Van Leeuwen, Piet W. N. M.,Vogt, Dieter

, p. 1496 - 1504 (2007/10/03)

New chiral aminophosphine phosphinite ligands with a stereogenic center at the aminophosphine phosphorus atom were prepared based on (R,S)-ephedrine as the chiral auxiliary and backbone. Substituents at the chiral aminophosphine as well as at the phosphinite phosphorus atom were varied. These new ligands were applied to the rhodium-catalyzed asymmetric hydroformylation of vinyl arenes. The enantiomeric excess reached up to 77%. 1H and 31P NMR studies of the Rh complexes under syngas pressure reveal that [HRh(CO)2(P/P)] complexes with the NP* moiety in an axial position are responsible for enantioselectivity.

Highly selective synthesis of 4-vinylcyclohexene by cyclodimerization of butadiene catalysed by aminophosphinephosphinite and bis(aminophosphine) chiral ligands nickel complexes

Suisse, Isabelle,Bricout, Herve,Mortreux, Andre

, p. 413 - 416 (2007/10/02)

The highest chemoselective synthesis of 4-vinylcyclohexene ever observed by butadiene cyclodimerization on nickel complexes has been obtained with aminophosphinephosphinite and bis(aminophosphine) chiral ligands (selectivity up to 99%).

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