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diethyl ((N-methyl-phenylamino)(phenyl)methyl)phosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104541-79-9

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104541-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104541-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,4 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104541-79:
(8*1)+(7*0)+(6*4)+(5*5)+(4*4)+(3*1)+(2*7)+(1*9)=99
99 % 10 = 9
So 104541-79-9 is a valid CAS Registry Number.

104541-79-9Downstream Products

104541-79-9Relevant academic research and scientific papers

Silica gel and polystyrene supported aluminum chloride as heterogeneous catalysts for the preparation of α-aminophosphonates

Boroujeni, Kaveh Parvanak,Shirazi, Amir Nasrolahi

, p. 418 - 422 (2010)

Silica gel supported aluminum chloride (SiO2-AlCl3) and cross-linked polystyrene-supported aluminum chloride (PS-AlCl3) are environment- friendly heterogeneous catalysts for the condensation of amines and aldehydes with diethyl phosphite to afford α-aminophosphonates. These solid acid catalysts are stable (as bench top catalysts) and can be easily recovered and reused without appreciable change in their efficiency.

Synthesis of α-Aminophosphonates via Phosphonylation of an Aryne-Imine Adduct

Lim, Taehyun,Kim, Byeong Moon

, p. 13246 - 13255 (2020)

Multicomponent phosphonylation is accomplished upon the reaction of an imine with an aryne generated in situ in the presence of a dialkyl phosphite. This transition-metal-free protocol shows a broad substrate scope, providing a variety of α-aminophosphonates in moderate to good yields. A plausible mechanism for the reaction is proposed based on a deuterium exchange experiment.

A simple protocol for the synthesis of α-substituted phosphonates

Wang, Xing,Cai, Yuan,Chen, Jian,Verpoort, Francis

, p. 1268 - 1273 (2016/08/31)

An efficient, easy-to-handle, and mild substitution reaction approach has been developed for the synthesis of phosphonate derivatives, which are very important in the field of industrial, agricultural, and medicinal chemistry. A large number of nucleophiles, including arylamines, alkylamines, heteroarylamines, primary amines and secondary amines, sulfides, and carbides were attempted to react with α-tosyloxyphosphonate 1. The reaction proceeded under catalyst-free and neat conditions and the corresponding phosphonates 2 were afforded in good yields.

Synthesis of α-aminophosphonates using polystyrene supported Al(OTf)3 as a heterogeneous catalyst

Boroujeni, Kaveh Parvanak

experimental part, p. 173 - 176 (2011/04/25)

A mild and efficient method has been devised for the preparation of -aminophosphonates from three component condensation of an aldehyde, an amine, and diethyl phosphite in the presence of catalytic amounts of cross-linked polystyrene supported aluminium triflate (Ps-Al(OTf)3) under solvent-free conditions in good to excellent yields. The catalyst is stable (as a bench top catalyst) and can be easily recovered and reused without appreciable change in its efficiency. Taylor & Francis Group, LLC.

Design and one-pot synthesis of α-aminophosphonates and bis(α-aminophosphonates) by iron(III) chloride and cytotoxic activity

Rezaei, Zahra,Firouzabadi, Habib,Iranpoor, Nasser,Ghaderi, Abbas,Jafari, Mohammad Reza,Jafari, Abbas Ali,Zare, Hamid Reza

experimental part, p. 4266 - 4275 (2009/12/24)

In this study, we used a solution of FeCl3 in THF to facilitate the Mannich-type reaction of aldehyde, amine and phosphite compounds to form corresponding α-aminophosphonates in a one-pot, three-component reaction. Selected α-aminophosphonates

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