74975-53-4 Usage
Uses
Used in Organic Synthesis:
1-(4-methoxyphenyl)non-1-en-3-one is used as a key intermediate for the synthesis of various organic compounds, leveraging its unique chemical properties to facilitate the creation of a wide range of products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(4-methoxyphenyl)non-1-en-3-one serves as a valuable compound for research purposes. Its potential biological activities make it a candidate for the development of new drugs and therapeutic agents.
Used as a Building Block for Chemical Production:
This enone compound is utilized as a fundamental building block in the production of a variety of chemicals, contributing to the diversification of chemical products and applications.
Used in Medicinal Chemistry Studies:
1-(4-methoxyphenyl)non-1-en-3-one is employed in medicinal chemistry as a subject of study for its potential biological activities. Researchers are interested in exploring its properties to understand its implications in the development of novel pharmaceuticals and therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 74975-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,7 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74975-53:
(7*7)+(6*4)+(5*9)+(4*7)+(3*5)+(2*5)+(1*3)=174
174 % 10 = 4
So 74975-53-4 is a valid CAS Registry Number.
74975-53-4Relevant academic research and scientific papers
An access to α, β-unsaturated ketones via dual cooperative catalysis
Syamala, Lakshmi V.R. Babu,Khopade, Tushar M.,Warghude, Prakash K.,Bhat, Ramakrishna G.
supporting information, p. 88 - 91 (2018/12/05)
A dual cooperative organocatalytic approach for the synthesis of α, β-unsaturated ketones is described. This one pot transformation is realized via a domino Knoevenagel-Michael-retro Michael reaction sequence. Various aliphatic ketones reacted smoothly with aromatic as well as aliphatic aldehydes in presence catalytic amount of Meldrum's acid and bifunctional amine. The highlights of this protocol are the easy availability of catalysts, high selectivity, and functional group tolerance. The reaction proved to highly E-selective with no side products emanating from self-condensation, unlike the base-mediated reactions.
