100573-60-2 Usage
Uses
Used in Pharmaceutical Industry:
(E)-2-(1-Ethoxy-ethoxy)-4-phenyl-but-2-enenitrile is used as an intermediate in the synthesis of pharmaceuticals for its ability to undergo various reactions to create complex organic molecules. It plays a crucial role in the development of new drugs and medicines.
Used in Agrochemical Industry:
(E)-2-(1-Ethoxy-ethoxy)-4-phenyl-but-2-enenitrile is also used as an intermediate in the synthesis of agrochemicals, contributing to the development of pesticides and other agricultural products.
Used in Organic Synthesis:
(E)-2-(1-Ethoxy-ethoxy)-4-phenyl-but-2-enenitrile is used as a versatile building block in organic synthesis, allowing for the creation of a wide range of organic compounds through various chemical reactions.
Used in Research Laboratories:
(E)-2-(1-Ethoxy-ethoxy)-4-phenyl-but-2-enenitrile is commonly used in research laboratories for its ability to undergo various reactions to create complex organic molecules, aiding in the advancement of scientific knowledge and the development of new chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 100573-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,7 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100573-60:
(8*1)+(7*0)+(6*0)+(5*5)+(4*7)+(3*3)+(2*6)+(1*0)=82
82 % 10 = 2
So 100573-60-2 is a valid CAS Registry Number.
100573-60-2Relevant academic research and scientific papers
Trimethylsilyl Cyanide - A Reagent for Umpolung, XI. On the Ambident Character of Substituted Allylic Anions.
Huenig, Siegfried,Reichelt, Helmut
, p. 1772 - 1800 (2007/10/02)
The dependence of the α/γ-ratio of alkylation products on several factors has been determined with 1-cyano-3-aryl-1-(trimethylsiloxy)allylic anions.Increasing amounts of γ-product are found in more polar solvents, with larger alkali ions, on addition of HMPT, with smaller alkyl groups in the electrophile, and especially with p-cyanophenyl groups.In contrast, temperature and leaving groups have minor effects.On substitution of the O-silyl group by O-methyl and O-ethoxycarbonyl, α-alkylation predominates strongly.The results are compared to known allylic anions.Furthermore, the isomerisation of compounds of type C to type B is described as well as a new addition reaction of cyanoformates to aldehydes.
