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(+/-)-diisopropyl 2-hydroxy-2-phenylethylphosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72019-17-1

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72019-17-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72019-17-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,1 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 72019-17:
(7*7)+(6*2)+(5*0)+(4*1)+(3*9)+(2*1)+(1*7)=101
101 % 10 = 1
So 72019-17-1 is a valid CAS Registry Number.

72019-17-1Relevant academic research and scientific papers

A β - hydroxyalkanephosphonic ester derivatives

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Paragraph 0055-0059, (2017/08/31)

The invention discloses a preparation method of beta-hydroxyphosphonate derivatives. The preparation method comprises that an arylethene derivative, a phosphorus reagent and manganese acetate are dissolved in a solvent and the solution undergoes a reactio

Mn(OAc)3-mediated synthesis of β-hydroxyphosphonates from P(O)-H compounds and alkenes

Gao, Yuzhen,Wu, Ju,Xu, Jian,Zhang, Pengbo,Tang, Guo,Zhao, Yufen

, p. 51776 - 51779 (2014/12/10)

A new and general method for the synthesis of β-hydroxy phosphonates has been achieved through Mn(OAc)3-mediated radical oxidative phosphonation of alkenes with H-phosphonates and H-phosphine oxide. The starting materials of P(O)-H compounds and alkenes are stable and cheap. Mn(OAc)3 can be readily prepared from Mn(OAc)2 in the laboratory. This method can be easily adapted to large-scale preparations. This journal is

Nonenzymatic kinetic resolution of racemic β-hydroxyalkanephosphonates with a chiral copper catalyst

Moriyama, Atsushi,Matsumura, Shintaro,Kuriyama, Masami,Onomura, Osamu

experimental part, p. 810 - 824 (2010/11/04)

Kinetic resolution of β-hydroxyalkanephosphonates was efficiently performed by 2-fluorobenzoylation in the presence of copper(II) triflate and (R,R)-Ph-BOX as a catalyst with good s value of up to 21.

Enzymes in Organic Chemistry, 11:[1] Hydrolase-Catalyzed Resolution of α- and β-Hydroxyphosphonates and Synthesis of Chiral, Non-Racemic β-Aminophosphonic Acids

Woschek,Lindner, Wolfgang,Hammerschmidt

, p. 1287 - 1298 (2007/10/03)

The enantioselective acylation of racemic diisopropyl α- and β-hydroxyphosphonates by hydrolases in t-butyl methyl ether with isopropenyl acetate as acyl donor is limited by the narrow substrate specificity of the enzymes. High enantiomeric excesses (up t

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