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dimethyl (1-(4-chlorophenyl)-1-hydroxyethyl)phosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

401610-08-0

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401610-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 401610-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,1,6,1 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 401610-08:
(8*4)+(7*0)+(6*1)+(5*6)+(4*1)+(3*0)+(2*0)+(1*8)=80
80 % 10 = 0
So 401610-08-0 is a valid CAS Registry Number.

401610-08-0Downstream Products

401610-08-0Relevant academic research and scientific papers

The catalytic aerobic synthesis of quaternary α-hydroxy phosphonates via direct hydroxylation of phosphonate compounds

Gu, Lijun,Jin, Cheng,Zhang, Hongtao

supporting information, p. 1579 - 1582 (2015/03/18)

A highly efficient Cu-catalyzed direct hydroxylation of phosphonate compounds has been developed. This transformation provides a powerful method for the synthesis of quaternary α-hydroxy phosphonates in good yields. The direct transformation process, regiospecific selectivity, and good tolerance to a variety of substituents make it an alternative approach to the reported protocols.

Synthesis of quaternary α-hydroxy phosphonates via direct hydroxylation of phosphonate compounds

Liu, Jiyan,Wang, Wei,Wang, Rui,Gu, Lijun

supporting information, p. 559 - 562 (2015/05/27)

It was found for the first time that Cs2CO3 serves as highly efficient catalyst for the direct hydroxylation reactions of phosphonates under mild conditions. This reaction provides an efficient approach to quaternary α-hydroxy phosph

C-H hydroxylation of phosphonates with oxygen in [bmIm]OH to produce quaternary α-hydroxy phosphonates

Li, Xiangguang,Jin, Cheng,Gu, Lijun

, p. 2443 - 2447 (2015/05/04)

A highly efficient and mild [bmIm]OH-catalyzed α-hydroxylation of phosphonates using O2 as the oxygen source is described. The employment of ionic liquid under mild reaction conditions makes this transformation green and practical. Especially, this reaction provided a novel and convenient methodology for the construction of quaternary α-hydroxy phosphonates.

Solvent-free synthesis of Tertiaryα-Hydroxyphosphates by the Triethylamine-catalyzed hydrophosphonylation of ketones

Wang, Chubei,Zhou, Jianwei,Lv, Xingbin,Wen, Junlei,He, Hongwu

, p. 1334 - 1339 (2013/10/08)

A new, environmentally benign, convenient, and easy method of synthesizing tertiary α-hydroxyphosphonates by the triethylamine-catalyzed hydrophosphonylation of unactivated ketones was developed. In the presence of triethylamine, aromatic or heteroaromati

Reactions of acyl phosphonates with organoaluminum reagents: A new method for the synthesis of secondary and tertiary α-hydroxy phosphonates

Seven, Ozlem,Polat-Cakir, Sidika,Hossain, Md. Shakhawoat,Emrullahoglu, Mustafa,Demir, Ayhan S.

, p. 3464 - 3469 (2011/06/19)

The reactions of organoaluminum reagents (trimethylaluminum, triethylaluminum, etc.) with aryl and alkyl acyl phosphonates, which lead to the formation of α-hydroxy phosphonates in moderate to good yields, are reported. This method provides easy access to

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