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Phosphonic acid, [(hydroxyimino)phenylmethyl]-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57353-44-3

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57353-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57353-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,5 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57353-44:
(7*5)+(6*7)+(5*3)+(4*5)+(3*3)+(2*4)+(1*4)=133
133 % 10 = 3
So 57353-44-3 is a valid CAS Registry Number.

57353-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[diethoxyphosphoryl(phenyl)methylidene]hydroxylamine

1.2 Other means of identification

Product number -
Other names diethyl 1-hydroxyiminobenzylphosphonate

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:57353-44-3 SDS

57353-44-3Relevant academic research and scientific papers

Visible photocatalysis of novel oxime phosphonates: Synthesis of β-aminophosphonates

Li, Yong-Hong,Wang, Chun-Hai,Gao, Su-Qian,Qi, Feng-Ming,Yang, Shang-Dong

supporting information, p. 11888 - 11891 (2019/10/11)

A novel type of oxime phosphonate was synthesized and used in the intermolecular cascade radical addition reaction of alkenes to access β-aminophosphonates via visible-light-driven N-centered iminyl radical-mediated and redox-neutral selective C-P single-bond cleavage in an active phosphorus radical route. The procedure is characterized by its ability to achieve the construction of Csp3-P and Csp3-N bonds without the requirement for oxidants and bases.

Visible-Light-Catalyzed Phosphonation-Annulation: an Efficient Strategy to Synthesize β-Phosphonopyrrolidines and β-Phosphonolactones

Li, Chong,Qi, Zhi-Chao,Yang, Qiang,Qiang, Xiao-Yue,Yang, Shang-Dong

supporting information, p. 1052 - 1058 (2018/09/25)

A new type of phosphine radical precursor for C—P bond formation has been developed and successfully used in visible-light-catalyzed phosphonation-annulation of unsaturated sulfonamides and carboxylic acids. The catalytic process is simple and green acces

Studies on organophosphorus compounds; LXXV: A facile synthesis of 1-(hydroxyamino)alkyl(or aryl)phosphonic acids

Yuan,Chen,Zhou,Maier

, p. 955 - 957 (2007/10/02)

Reduction of dialkyl 1-(hydroxyimino)alkyl(aryl)phosphonate 1 with borane-pyridine complex proceeds smoothly to give dialkyl 1-(hydroxyamino)alkyl(or aryl)phosphonate 2 which is then easily converted into the corresponding hydroxyaminophosphonic acid 3 by

31P Hyperfine Interaction in a New Type of Phosphorus-Containing Iminoxy Free Radicals. An ESR Study

Siatecki, Zdzislaw,Chmielewski, Piotr J.,Jezierski, Adam

, p. 163 - 168 (2007/10/02)

Iminoxy radicals of a new type, having the general formula RC(=NO.)P(O)(OEt)2, were synthesized and characterized by means of ESR spectroscopy.The presence of two isomers due to the different position of the C=NO. fragment with respe

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