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diisopropyl (4-methylphenylsulfonamido)(phenyl)methylphosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84454-07-9

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84454-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84454-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,5 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84454-07:
(7*8)+(6*4)+(5*4)+(4*5)+(3*4)+(2*0)+(1*7)=139
139 % 10 = 9
So 84454-07-9 is a valid CAS Registry Number.

84454-07-9Relevant academic research and scientific papers

Enantioselective Synthesis of α-Amino Phosphonates via Pd-Catalyzed Asymmetric Hydrogenation

Yan, Zhong,Wu, Bo,Gao, Xiang,Chen, Mu-Wang,Zhou, Yong-Gui

, p. 692 - 695 (2016)

A highly enantioselective palladium-catalyzed hydrogenation of a series of linear and cyclic α-iminophosphonates has been achieved, providing efficient access to optically active α-aminophosphonates with up to 99% ee. (Chemical Equation Presented).

Asymmetric synthesis of functionalized tetrasubstituted α-aminophosphonates through enantioselective aza-Henry reaction of phosphorylated ketimines

Vicario, Javier,Ortiz, Pablo,Ezpeleta, José M.,Palacios, Francisco

, p. 156 - 164 (2016/09/09)

Bifunctional Cinchona alkaloid thioureas efficiently catalyze asymmetric nucleophilic addition of nitromethane to ketimines derived from α-aminophosphonic acids to afford tetrasubstituted α-amino-β-nitro-phosphonates. Catalytic hydrogenation of (S)-α-amin

Asymmetric cyanation of a-ketiminophosphonates catalyzed by cinchona alkaloids: Enantioselective synthesis of tetrasubstituted a-aminophosphonic acid derivatives from trisubstituted a-aminophosphonates

Vicario, Javier,Ezpeleta, Jose Mari,Palacios, Francisco

, p. 2641 - 2647 (2013/01/15)

An enantioselective synthesis of tetrasubstituted a-phosphono-a-amino nitriles through asymmetric cyanation of a-ketiminophosphonates catalyzed by Cinchona alkaloids is reported. a-Ket- ACHTUNGTRENUNGiminophosphonates are generated, in a very efficient sy

A Facile Synthesis of O,O-Dialkyl-α-(p-toluenesulphonamido)-benzyl Phosphonates

Varaprasad, I. V. S.,Jaiswal, D. K.

, p. 525 - 527 (2007/10/02)

A series of O,O-dialkyl-α-(p-toluenesulphonamido)benzyl phosphonates have been synthesised by the addition of alkyl phosphites to N-benzylidene-p-toluenesulphonamide.The compounds exhibit chemical shift nonequivalence of prochiral alkoxy groups.Furthermore, on the basis of observed 2JPCH, a preferred conformation with benzylic hydrogen in gauche-disposition to phosphoryl group has been suggested.

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