5325-89-3 Usage
Description
(2E)-1-(4-aminophenyl)-3-pyridin-2-ylprop-2-en-1-one is an organic compound with the molecular formula C14H12N2O. It is a yellow solid that is insoluble in water but soluble in organic solvents. (2E)-1-(4-aminophenyl)-3-pyridin-2-ylprop-2-en-1-one is a derivative of pyridine and contains a prop-2-en-1-one functional group. Its unique structural features and potential biological activities make it a promising candidate for applications in medicinal chemistry and pharmaceutical research. However, further research and testing are required to fully understand its potential uses and properties.
Uses
Used in Medicinal Chemistry:
(2E)-1-(4-aminophenyl)-3-pyridin-2-ylprop-2-en-1-one is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its structural features and potential biological activities make it a valuable building block in the development of new drugs.
Used in Pharmaceutical Research:
(2E)-1-(4-aminophenyl)-3-pyridin-2-ylprop-2-en-1-one is used as a research tool in pharmaceutical research to investigate its potential biological activities and therapeutic effects. Its unique structure and properties may contribute to the discovery of new drugs and treatments for various diseases.
Used in Drug Development:
(2E)-1-(4-aminophenyl)-3-pyridin-2-ylprop-2-en-1-one is used as a starting material in the development of new drugs. Its potential applications in medicinal chemistry and pharmaceutical research make it a valuable compound for further exploration and optimization to create effective and safe medications.
Used in Chemical Synthesis:
(2E)-1-(4-aminophenyl)-3-pyridin-2-ylprop-2-en-1-one is used as a reactant in various chemical synthesis processes. Its reactivity and functional groups make it a versatile building block for the creation of new organic compounds and materials.
Used in Analytical Chemistry:
(2E)-1-(4-aminophenyl)-3-pyridin-2-ylprop-2-en-1-one is used as an analytical standard or reference compound in analytical chemistry. Its unique properties and characteristics can be used to calibrate instruments, validate analytical methods, and ensure the accuracy of measurements in various chemical analyses.
Used in Material Science:
(2E)-1-(4-aminophenyl)-3-pyridin-2-ylprop-2-en-1-one may have potential applications in material science, such as the development of new materials with specific properties or functions. Its structural features and potential interactions with other compounds make it a candidate for further exploration in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 5325-89-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5325-89:
(6*5)+(5*3)+(4*2)+(3*5)+(2*8)+(1*9)=93
93 % 10 = 3
So 5325-89-3 is a valid CAS Registry Number.
5325-89-3Relevant articles and documents
Design, synthesis, docking and biological evaluation of chalcones as promising antidiabetic agents
Bhaskar, Baki Vijaya,Gu, Wei,Rammohan, Aluru,Venkateswarlu, Nagam,Zyryanov, Grigory V.
, (2020/01/08)
Diabetes mellitus (DM) is a serious chronic metabolic disorder which occurs due to dysfunction of insulin and therapeutic approaches are poor. It is an under estimation that 387 million people currently suffering globally with diabetic and more than 592 m
Design, synthesis, molecular modeling, and ADMET studies of some pyrazoline derivatives as shikimate kinase inhibitors
James, Jainey P.,Ishwar Bhat,More, Uttam A.,Joshi, Shrinivas D.
, p. 546 - 559 (2017/11/16)
A series of pyrazoline derivatives were synthesized and their structures have been characterized by IR, 1H NMR, 13C NMR, mass spectral and elemental analysis. The novel compounds were designed as Mycobacterium tuberculosis shikimate
In vitro antioxidant activity and scavenging effects of some synthesized 4-Aminochalcones
Prasad, Y.Rajendra,Rani, V. Jhansi,Rao, A. Srinivasa
, p. 52 - 58 (2013/02/22)
A new series of substituted 4'-aminochalcones were synthesized by Claisen-Schmidt condensation of 4-aminoacetophenone with various substituted aromatic/heteroaromatic aldehydes. The antioxidant activity for all these compounds were studied on various reac
