64953-82-8 Usage
Uses
Used in Pharmaceutical Industry:
2-Chloro-1-(4-ethoxyphenyl)ethanone is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into the molecular structures of different drugs.
Used in Agrochemical Industry:
2-Chloro-1-(4-ethoxyphenyl)ethanone 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:
2-Chloro-1-(4-ethoxyphenyl)ethanone is utilized in organic synthesis for the preparation of various organic compounds, taking advantage of its reactivity and functional groups.
It is important to handle 2-Chloro-1-(4-ethoxyphenyl)ethanone with care, as it is considered to be hazardous and may cause skin and eye irritation, as well as respiratory issues if inhaled.
Check Digit Verification of cas no
The CAS Registry Mumber 64953-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,5 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64953-82:
(7*6)+(6*4)+(5*9)+(4*5)+(3*3)+(2*8)+(1*2)=158
158 % 10 = 8
So 64953-82-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO2/c1-2-13-9-5-3-8(4-6-9)10(12)7-11/h3-6H,2,7H2,1H3
64953-82-8Relevant academic research and scientific papers
Kinetics of Oxidation of Ketones by Trichloroisocyanuric Acid in Acid Medium: Anomalous Behaviour of Alkoxyacetophenones
Radhakrishnamurti, P. S.,Rath, Nabeen Kumar
, p. 300 - 303 (2007/10/02)
Kinetics of oxidation of aliphatic, aryl aliphatic and cyclic ketones by trichloroisocyanuric acid has been studied in aqueous acetic acid medium in the presence of HClO4.The reaction is acid-catalysed exhibiting first order dependence each in and and zero order dependence in .This supports the acid catalyzed enolisation of ketone as the rate-determining step and reaction between enol and oxidant as the fast step.Alkoxyacetophenones exhibit an anomalous behaviour in that there is first order dependence on the halogenating agent.This has been attributed to the fact that in the case of alkoxyacetophenones the rates of halogenation may be less than the rates of enolisation.The decrease in dielectric constant of the medium slightly enhances the rate of reaction.The ρ? relationship in the case of acetophenones is linear with ρ as -0.2 indicating the simultaneous operation of equilibrium protonation of ketone and deprotonation of conjugate acid.Arrhenius activation parameters have been computed.A plausible mechanism consistent with the experimental results is postulated.
