3769-99-1 Usage
Uses
Used in Pharmaceutical Research:
Ethanone, 2-(4-nitrophenyl)-1-(3-pyridinyl)-, is used as a research compound for its potential as a drug target. It is particularly valuable in the development of treatments for cancer, inflammation, and neurological disorders due to its unique chemical structure and properties.
Used in Chemical Synthesis:
In the chemical industry, Ethanone, 2-(4-nitrophenyl)-1-(3-pyridinyl)-, is utilized as a reagent or intermediate in the synthesis of other compounds. Its versatile structure allows for its use in a variety of chemical reactions, contributing to the creation of new and innovative products.
Used in Laboratory Settings:
Ethanone, 2-(4-nitrophenyl)-1-(3-pyridinyl)-, is also employed in laboratory settings for various experiments and analyses. Its properties make it suitable for use in a range of scientific applications, from testing hypotheses to developing new methodologies.
Used in Drug Development:
Ethanone, 2-(4-nitrophenyl)-1-(3-pyridinyl)is of interest for further exploration and research in the development of new treatments and therapies. Its potential pharmacological properties are being studied to understand its mechanisms of action and to identify how it can be effectively used in medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 3769-99-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,6 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3769-99:
(6*3)+(5*7)+(4*6)+(3*9)+(2*9)+(1*9)=131
131 % 10 = 1
So 3769-99-1 is a valid CAS Registry Number.
3769-99-1Relevant academic research and scientific papers
An improved and practical procedure for the synthesis of substituted phenylacetylpyridines
Journet, Michel,Cai, Dongwei,Larsen, Robert D.,Reider, Paul J.
, p. 1717 - 1720 (2007/10/03)
A general procedure for the synthesis of substituted phenylacetylpyridines in excellent yields is described using a Horner-Emmons condensation between α-aminoalkylphosphonates of pyridinecarboxaldehydes and benzaldehydes with cesium carbonate at room temperature.
