2404-75-3 Usage
Uses
Used in Pharmaceutical and Agrochemical Production:
DIETHYL N-BUTANEPHOSPHONATE is used as a chemical intermediate for the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new and effective products in these industries.
Used in Polymer and Resin Industries:
DIETHYL N-BUTANEPHOSPHONATE is used as a flame retardant in polymers and resins, providing high heat resistance and enhancing the safety and performance of these materials.
Used in Insecticide Manufacturing:
DIETHYL N-BUTANEPHOSPHONATE is used in the manufacture of insecticides, serving as a key component in the development of effective pest control products.
Used in Chemical Synthesis:
DIETHYL N-BUTANEPHOSPHONATE is used as a chemical intermediate in the synthesis of various compounds, playing a crucial role in the production of a wide range of chemical products.
It is important to handle DIETHYL N-BUTANEPHOSPHONATE with caution, as it is toxic and can pose health risks if not handled properly.
Check Digit Verification of cas no
The CAS Registry Mumber 2404-75-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,0 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2404-75:
(6*2)+(5*4)+(4*0)+(3*4)+(2*7)+(1*5)=63
63 % 10 = 3
So 2404-75-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H19O3P/c1-4-7-8-12(9,10-5-2)11-6-3/h4-8H2,1-3H3
2404-75-3Relevant academic research and scientific papers
Stereochemical consequences of the use of chiral N-phosphoryl oxazolidinones in the attempted kinetic resolution of bromomagnesium alkoxides
Jones, Simon,Selitsianos, Dimitrios
, p. 3128 - 3138 (2007/10/03)
A number of chiral N-phosphoryl oxazolidinones have been prepared and evaluated as asymmetric phosphoryl transfer agents with the magnesium alkoxide of 1-phenyl ethanol. The reaction proceeded with little stereoselection, which was shown to be a consequence of the reaction mechanism that occurs with inversion of configuration at phosphorus consistent with in-line attack opposite the leaving group.
Microwave irradiation in organophosphorus chemistry 1: The Michaelis-Arbuzov reaction
Kiddle, James J.,Gurley, Alison F.
, p. 195 - 205 (2007/10/03)
A diverse series of phosphonate esters have been prepared using a domestic microwave oven. The microwave enhanced Michaelis-Arbuzov reaction shows remarkable rate acceleration under microwave irradiation and allows the facile synthesis, and in certain cases easy workup, of alkyl, α-substituted and aryl phosphonates.
