41327-48-4 Usage
Uses
Used in Pharmaceutical Industry:
(2-PHENYLCARBAMOYL-PHENYL)-PHOSPHONIC ACID DIETHYL ESTER is used as a potential candidate in the development of new drugs due to its unique chemical structure and properties.
Used in Chemical Synthesis:
(2-PHENYLCARBAMOYL-PHENYL)-PHOSPHONIC ACID DIETHYL ESTER is used as an intermediate in the synthesis of other chemical compounds, contributing to the creation of various products in the chemical industry.
It is important to handle and use (2-PHENYLCARBAMOYL-PHENYL)-PHOSPHONIC ACID DIETHYL ESTER with caution, following proper safety guidelines and protocols due to its potential reactivity and toxicity.
Check Digit Verification of cas no
The CAS Registry Mumber 41327-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,2 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41327-48:
(7*4)+(6*1)+(5*3)+(4*2)+(3*7)+(2*4)+(1*8)=94
94 % 10 = 4
So 41327-48-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H20NO4P/c1-3-21-23(20,22-4-2)16-13-9-8-12-15(16)17(19)18-14-10-6-5-7-11-14/h5-13H,3-4H2,1-2H3,(H,18,19)
41327-48-4Relevant academic research and scientific papers
Visible-light-induced denitrogenative phosphorylation of benzotriazinones: A metal- And additive-free method for accessing: Ortho -phosphorylated benzamide derivatives
Chen, Fushan,Hu, Shanshan,Li, Sipei,Tang, Guo,Zhao, Yufen
, p. 296 - 301 (2021/01/28)
Metal-free, visible-light-induced denitrogenative phosphorylation of 1,2,3-benzotriazinones was achieved. With the use of eosin Y as a photoredox catalyst, N,N-diisopropylethylamine as a base, CH3CN-H2O as a solvent and sunlight or a blue LED as a light source, a variety of aryl-phosphonates, aryl-phosphinates, and aryl-phosphine oxides were efficiently prepared. In addition, B2pin2 instead of P-nucleophiles as a radical acceptor was also demonstrated. The key advantages of this newly developed method are the clean reaction profile, use of a low-cost organic-dye catalyst, energy efficiency, broad substrate scope, good to excellent yields and large-scale synthetic applicability. The gram-scale synthesised compounds could be isolated in pure form just upon extraction, followed by re-crystallisation; no tedious chromatographic purification was required.
