37612-59-2 Usage
Uses
Used in Pharmaceutical Industry:
1-(3-chloro-4-ethoxyphenyl)ethanone is used as a key intermediate in the synthesis of pharmaceutical products for its ability to be incorporated into complex organic molecules, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(3-chloro-4-ethoxyphenyl)ethanone is utilized as a building block in the creation of agrochemicals, playing a crucial role in the formulation of pesticides and other agricultural chemicals to enhance crop protection and yield.
Used in Organic Synthesis:
1-(3-chloro-4-ethoxyphenyl)ethanone is employed as a versatile building block in organic synthesis, allowing for the construction of a wide range of organic compounds with diverse applications across various industries.
Used in Chiral Catalysts Production:
1-(3-chloro-4-ethoxyphenyl)ethanone is used as a precursor in the synthesis of chiral catalysts, which are essential in asymmetric synthesis to produce enantiomerically pure compounds, a critical aspect in the production of high-quality pharmaceuticals and fine chemicals.
Used in Antimicrobial and Anti-infective Applications:
Due to its antimicrobial and anti-infective properties, 1-(3-chloro-4-ethoxyphenyl)ethanone is utilized in the development of products that combat microbial infections, contributing to the field of infectious disease control and prevention.
Check Digit Verification of cas no
The CAS Registry Mumber 37612-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,1 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37612-59:
(7*3)+(6*7)+(5*6)+(4*1)+(3*2)+(2*5)+(1*9)=122
122 % 10 = 2
So 37612-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO2/c1-3-13-10-5-4-8(7(2)12)6-9(10)11/h4-6H,3H2,1-2H3
37612-59-2Relevant academic research and scientific papers
Room temperature C(sp2)-H oxidative chlorination: Via photoredox catalysis
Zhang, Lei,Hu, Xile
, p. 7009 - 7013 (2017/10/05)
Photoredox catalysis has been developed to achieve oxidative C-H chlorination of aromatic compounds using NaCl as the chlorine source and Na2S2O8 as the oxidant. The reactions occur at room temperature and exhibit exclusive selectivity for C(sp2)-H bonds over C(sp3)-H bonds. The method has been used for the chlorination of a diverse set of substrates, including the expedited synthesis of key intermediates to bioactive compounds and a drug.
