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diethyl α,α-difluoro-2-nitrobenzylphosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

177284-52-5

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177284-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177284-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,2,8 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 177284-52:
(8*1)+(7*7)+(6*7)+(5*2)+(4*8)+(3*4)+(2*5)+(1*2)=165
165 % 10 = 5
So 177284-52-5 is a valid CAS Registry Number.

177284-52-5Relevant academic research and scientific papers

Copper-Mediated Introduction of the CF2PO(OEt)2 Motif: Scope and Limitations

Ivanova, Maria V.,Bayle, Alexandre,Besset, Tatiana,Pannecoucke, Xavier,Poisson, Thomas

, p. 17318 - 17338 (2017/11/20)

Herein, a general procedure to access CF2PO(OEt)2-containing molecules is reported. The reagent CuCF2PO(OEt)2 is accessible by a simple protocol and a broad range of substrates can be functionalised. The procedure allows the conversion of aryl diazonium salts, as well as aryl, heteroaryl, vinyl and alkynyl iodonium salts, into the corresponding fluorinated molecules at room temperature. Mechanistic studies were performed to gain a better understanding of the reaction pathway. Under similar conditions, vinyl and aryl iodides, allyl halides, and benzyl bromides were also functionalised, and the scope and limitations of the reaction were studied. Finally, the procedure was extended to disulfides to offer new access to SCF2PO(OEt)2-containing molecules.

Cuprous chloride promoted coupling reaction of diethoxyphosphinyldifluoromethylcadmium reagent with aryl iodides: A practical and convenient preparation of α,α-difluoro benzylic phosphonates

Qiu, Weiming,Burton, Donald J.

, p. 45 - 51 (2013/10/01)

The cross coupling reaction of diethoxyphosphinyldifluoromethylcadmium reagent with aryl iodides was promoted by CuCl under mild conditions to give α,α-difluoro benzylic phosphonates in good yields. A variety of functional groups, including halides, phosphonate, nitro, ketone, carboxylic acid and ester in aryl iodides, could be tolerated. This methodology has been successfully applied to prepare α,α-difluoro Fostedil 9.

AMIDES AS SPHINGOMYELINE INHIBITORS

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Page/Page column 58, (2008/06/13)

The present invention, relates to compounds of formula (I), wherein A is hydrogen or (C1-4)alkyl, R1 is a group Y-R2, Y is not present or is (C1-4)alkylene, which alkylene optionally is substituted, e.g. one or

Discovery of novel phosphonic acid derivatives as new chemical leads for inhibitors of TNF-α production

Matsui, Toshiaki,Takahashi, Shinya,Matsunaga, Naoki,Nakamura, Kazunori,Omawari, Nagashige,Sakai, Masaru,Kamoshima, Wataru,Terai, Kouichiro,Ohno, Hiroyuki,Obata, Takaaki,Nakai, Hisao,Toda, Masaaki

, p. 3807 - 3815 (2007/10/03)

2-(Acylamino)benzylphosphonic acid 6 derived from an artificial substrate of sphingomyelinase was found to show inhibitory activity of TNF-α production. Structural optimization was started with the chemical modification of 6. The discovery of another chem

A facile and general preparation of α,α-difluoro benzylic phosphonates by the CuCl promoted coupling reaction of the (diethylphosphonyl)difluoromethylcadmium reagent with aryl iodides

Qiu, Weiming,Burton, Donald J.

, p. 2745 - 2748 (2007/10/03)

A series of α,α-difluoro benzylic phosphonates have been prepared in good yield (65-88%) by the CuCl promoted coupling reaction of the (diethylphosphonyl)difluoromethylcadmium reagent with aryl iodides.

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