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(4-Methoxy-phenyl)-phosphonous acid diethyl ester is an organic compound with the chemical formula C11H17O3P. It is a colorless liquid that is soluble in organic solvents. (4-methoxy-phenyl)-phosphonous acid diethyl ester is a derivative of phosphonous acid, featuring a 4-methoxyphenyl group attached to the phosphorus atom. It is synthesized by reacting 4-methoxyphenol with diethyl phosphite. This chemical is primarily used as a reagent in organic synthesis, particularly in the formation of phosphonate esters and as a precursor to various phosphorus-containing compounds. It is also utilized in the preparation of agrochemicals and pharmaceuticals due to its ability to form stable intermediates in chemical reactions.

67103-60-0

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67103-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67103-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,1,0 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 67103-60:
(7*6)+(6*7)+(5*1)+(4*0)+(3*3)+(2*6)+(1*0)=110
110 % 10 = 0
So 67103-60-0 is a valid CAS Registry Number.

67103-60-0Relevant academic research and scientific papers

Efficient Synthesis of Phosphonamidates through One-Pot Sequential Reactions of Phosphonites with Iodine and Amines

Chen, Xunwei,Luo, Wenjun,Wang, Yanlin,Li, Zikang,Ma, Xiaorui,Peng, Ai-Yun

, p. 14474 - 14480 (2020/10/06)

A one-pot sequential strategy to construct phosphonamidates has been developed by generating phosphonites in situ from arylmagnesium bromides and triethyl phosphite followed by treatment with iodine and amines. A variety of phosphonamidates were obtained with good to excellent yields at room temperature from easily available materials.

Revisited synthesis of aryl-H-phosphinates

Volle, Jean-Noel,Filippini, Damien,Midrier, Camille,Sobecki, Michal,Drag, Marcin,Virieux, David,Pirat, Jean-Luc

experimental part, p. 2490 - 2494 (2011/09/20)

A systematic study of the reaction conditions for the preparation of pure aryl-H-phosphinate esters, originally developed by Sander and optimized by Petnehazy, is reported. The influence of the reaction concentration has been investigated for the formation of phosphonite intermediates via direct addition of triethyl phosphite to the appropriate Grignard reagent. Subsequent hydrolysis of the phosphonites under acidic conditions gives various aryl-H-phosphinates in high yields and purities. Georg Thieme Verlag Stuttgart, New York.

Nuclear magnetic resonance, luminescence and structural studies of lanthanide complexes with octadentate macrocyclic ligands bearing benzylphosphinate groups

Aime, Silvio,Batsanov, Andrei S.,Botta, Mauro,Dickins, Rachel S.,Faulkner, Stephen,Foster, Clive E.,Harrison, Alice,Howard, Judith A. K.,Moloney, Janet M.,Norman, Timothy J.,Parker, David,Royle, Louise,Williams, J. A. Gareth

, p. 3623 - 3636 (2007/10/03)

The solution and solid-state structures of lanthanide complexes of 1,4,7,10-tetraazacyclododecane-1,4,7,10- tetryltetramethylenetetra(benzylphosphinate), L1a, and of its o-, m- and p-methoxybenzyl analogues (L2, L3, L

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