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α-Hydroxy-3-nitrobenzylphosphonic acid diethyl ester is a complex organic compound with the chemical formula C11H14NO6P. It is a derivative of phosphonic acid, featuring a hydroxyl group (-OH), a nitro group (-NO2), and a benzyl group attached to the phosphonic acid backbone. The diethyl ester functional group (-OC2H5)2 is present, indicating that two of the hydroxyl groups in the phosphonic acid have been replaced by ethyl groups. α-Hydroxy-3-nitrobenzylphosphonic acid diethyl ester is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in materials science for the development of new polymers and other advanced materials. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable intermediate in organic synthesis.

50652-91-0

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50652-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50652-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,5 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50652-91:
(7*5)+(6*0)+(5*6)+(4*5)+(3*2)+(2*9)+(1*1)=110
110 % 10 = 0
So 50652-91-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H16NO6P/c1-3-17-19(16,18-4-2)11(13)9-6-5-7-10(8-9)12(14)15/h5-8,11,13H,3-4H2,1-2H3

50652-91-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name diethoxyphosphoryl-(3-nitrophenyl)methanol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:50652-91-0 SDS

50652-91-0Relevant academic research and scientific papers

A convenient and mild protocol for preparation of α – trimethylsilyloxyphosphonates using sulfamic acid and their oxidation to α – ketophosphonates in the presence of N-bromosuccinimide

Mitragotri, Satish D.,Kulkarni, Makarand A.,Desai, Uday V.,Wadagaonkar, Prakash P.

, (2021/10/05)

A convenient and mild protocol was developed for the trimethylsilylation of α-hydroxyphosphonates using hexamethyldisilazane as the silylating agent in the presence of sulfamic acid (SA) as a heterogeneous solid acid catalyst in dichloromethane as the rea

Method for synthesizing aromatic ring-containing alpha-hydroxyphosphonate through copper catalysis

-

Paragraph 0036-0038, (2020/05/01)

The invention relates to a method for synthesizing aromatic ring-containing alpha-hydroxyphosphonate through copper catalysis. The method comprises the following steps: dissolving diethyl phosphite and aromatic aldehyde in an organic solvent, adding a cop

Syntheses of bimetallic rare-earth bis(cyclopentadienyl) derivatives supported by bridged bis(guanidinate) ligands and their catalytic property for the hydrophosphonylation of aldehydes

Nie, Kun,Liu, Chengwei,Zhang, Yong,Yao, Yingming

, p. 59 - 65 (2016/01/15)

Some bimetallic rare earth bis(cyclopentadienyl) derivatives supported by bridged bis(guanidinate) ligands {(C5H5)2RE[(RN)2CN(CH2)2]}2 [R = iPr, RE = Yb(1), Er(2), Y(3

Synthesis and characterization of ytterbium guanidinates stabilized by bridged bis(phenolate) ligand and their application for the hydrophosphonylation reaction of aldehydes

Zeng, Tinghua,Qian, Qinqin,Wang, Yaorong,Yao, Yingming,Shen, Qi

, p. 14 - 20 (2015/02/18)

A series of ytterbium guanidinato complexes stabilized by an amine-bridged bis(phenolate) ligand were prepared, and their catalytic property for the hydrophosphonylation reaction of aldehydes was explored. Metathesis reactions of amine-bridged bis(phenola

Syntheses of bimetallic lanthanide bis(amido) complexes stabilized by bridged bis(guanidinate) ligands and their catalytic activity toward the hydrophosphonylation reaction of aldehydes and ketones

Nie, Kun,Liu, Chengwei,Zhang, Yong,Yao, Yingming

, p. 1451 - 1460 (2015/09/02)

A series of bimetallic lanthanide bis(amido) complexes stabilized by bridged bis(guanidinate) ligands {[(Me3Si)2N]2Ln[(RN)2-CN(CH2)2]}2 [R= i Pr, Ln=Sm (1), Yb (2), Y

MgO-coated-Fe3O4 nanoparticles as a magnetically recoverable and reusable catalyst for the synthesis of 1-hydroxyphosphonates

Kaboudin, Babak,Kazemi, Foad,Habibi, Fereshteh

, p. 469 - 475 (2015/02/05)

Nanosize magnetic particles coated with magnesium oxide (core/shell nanoparticles) have been prepared and used for the synthesis of 1-hydroxyalkyl phosphonates. Catalytic activity studies show that the magnetic particles coated with magnesium oxide have h

Lanthanide anilido complexes: Synthesis, characterization, and use as highly efficient catalysts for hydrophosphonylation of aldehydes and unactivated ketones

Liu, Chengwei,Qian, Qinqin,Nie, Kun,Wang, Yaorong,Shen, Qi,Yuan, Dan,Yao, Yingming

, p. 8355 - 8362 (2014/06/09)

Lanthanide anilido complexes stabilized by the 2,6-diisopropylanilido ligand have been synthesized and characterized, and their catalytic activity for hydrophosphonylation reaction was explored. A reaction of anhydrous LnCl 3 with 5 equivalents

N -BuLi as a highly efficient precatalyst for hydrophosphonylation of aldehydes and unactivated ketones

Liu, Chengwei,Zhang, Yu,Qian, Qinqin,Yuan, Dan,Yao, Yingming

supporting information, p. 6172 - 6175 (2015/01/09)

It was found for the first time that organic alkali metal compounds serve as highly efficient precatalysts for the hydrophosphonylation reactions of aldehydes and unactivated ketones with dialkyl phosphite under mild conditions. For ketone substrates, a reversible reaction was observed, and the influence of catalyst loading and reaction temperature on the reaction equilibrium was studied in detail. Overall, the hydrophosphonylation reactions catalyzed by 0.1 mol % n-BuLi were completed within 5 min for a broad range of substrates and generated a series of α-hydroxy phosphonates in high yields.

Synthesis, structure, and catalytic activity of novel trinuclear rare-earth metal amido complexes incorporating μ-η5:η1 bonding indolyl and μ3-oxo groups

Yang, Song,Zhu, Xiancui,Zhou, Shuangliu,Wang, Shaowu,Feng, Zhijun,Wei, Yun,Miao, Hui,Guo, Liping,Wang, Fenhua,Zhang, Guangchao,Gu, Xiaoxia,Mu, Xiaolong

supporting information, p. 2521 - 2533 (2014/02/14)

The reactions of different pyrrolyl-functionalized indoles with rare-earth metal(iii) amides [(Me3Si)2N]3RE III(μ-Cl)Li(THF)3 (RE = Yb, Er, Dy, Eu, Y) produced different kinds of rare-earth metal amid

Synthesis and characterization of amidate rare-earth metal amides and their catalytic activities toward hydrophosphonylation of aldehydes and unactivated ketones

Zhao, Lu,Ding, Hao,Zhao, Bei,Lu, Chengrong,Yao, Yingming

, p. 50 - 59 (2015/01/09)

Two novel amidate rare-earth metal amides Ln[N(SiMe3)2](κ2-L1)2(THF) (L1 = C6H5C(O)NC6H3(iPr)2) (Ln = Yb (1), Y (2)) were p

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