23040-22-4 Usage
Uses
Used in Pharmaceutical Industry:
(DIPHENYLPHOSPHORYL)ACETONITRILE is used as a chemical intermediate for the production of various pharmaceuticals. Its role in this industry is crucial as it aids in the synthesis of a wide range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, (DIPHENYLPHOSPHORYL)ACETONITRILE serves as a vital component in the creation of different agrochemicals. Its application in this industry helps in the development of products that protect crops from pests and diseases, ensuring increased agricultural productivity and food security.
Used in Organic Synthesis:
(DIPHENYLPHOSPHORYL)ACETONITRILE is also utilized in the synthesis of other organic compounds. Its versatility as a chemical intermediate makes it a valuable asset in the field of organic chemistry, where it can be employed to create a variety of molecules with diverse applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 23040-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,4 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23040-22:
(7*2)+(6*3)+(5*0)+(4*4)+(3*0)+(2*2)+(1*2)=54
54 % 10 = 4
So 23040-22-4 is a valid CAS Registry Number.
23040-22-4Relevant academic research and scientific papers
Regioselective lactonization of unsymmetrical 1,4-diols: An efficient access to lactone lignans
Ito, Masato,Shiibashi, Akira,Ikariya, Takao
supporting information; experimental part, p. 2134 - 2136 (2011/04/21)
A Cp*Ru-based bifunctional catalyst system (Cp* = η5-C5(CH3)5) with a suitably-designed PN ligand (PN = chelating tertiary phosphine-protic amine ligand) has been developed for a regioselective lactonization of
Synthesis of phosphane oxides and phosphonates by cerium-mediated addition of organolithium compounds to chloro-phosphorus compounds
Dalpozzo, Renato,De Nino, Antonio,Miele, Daniela,Tagarelli, Antonio,Bartoli, Giuseppe
, p. 2299 - 2301 (2007/10/03)
The addition of organocerium reagents 2a-g to phosphinoyl chloride 1a or chlorophosphates 1b leads to the synthesis of phosphane oxides 3aa-ag and phosphonates 3bb, be in good to high yield. The reaction can be extended to cerium enolates 4 (of ketones) and 6 (of nitriles) except when a benzyl group bound to the carbonyl moiety should be metallated. The latter reaction is the first reported synthesis of β-oxophosphane oxides by a simple reaction between enolates and a phosphorus(V) halide.
