91566-64-2 Usage
Type of compound
Synthetic chemical compound
Fields of potential applications
Medicine, pharmacology, and research
Functional group
Amide
Structural and chemical properties
+ Methyl group
+ Acetylamino group
+ Phenyl group
+ Prop-2-enamide backbone
Possible uses
Drug development, research tool, building block for synthesis of new chemical entities
Specific uses and properties
Vary depending on context and field of application
Check Digit Verification of cas no
The CAS Registry Mumber 91566-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,6 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91566-64:
(7*9)+(6*1)+(5*5)+(4*6)+(3*6)+(2*6)+(1*4)=152
152 % 10 = 2
So 91566-64-2 is a valid CAS Registry Number.
91566-64-2Relevant academic research and scientific papers
Facile synthesis of 4-arylidene-5-imidazolinones as synthetic analogs of fluorescent protein chromophore
Lee, Cheng-Yu,Chen, Yun-Chung,Lin, Hao-Chun,Jhong, Yuandong,Chang, Chih-Wei,Tsai, Ching-Hua,Kao, Chai-Lin,Chien, Tun-Cheng
, p. 5898 - 5907 (2012/09/07)
A facile and effective synthesis for a wide variety of 4-arylidene-5- imidazolinone derivatives was developed. 4-Arylidene-5-oxazolinones were prepared by Erlenmeyer azlactone synthesis from N-acylglycines and arylaldehydes. The ring-opening reactions of the 4-arylidene-5-oxazolinones with primary amines afforded 2-acylamino-3-arylacrylamides in excellent yields. A new dehydrative cyclization of the 2-acylamino-3-arylacrylamides in pyridine under reflux furnished the corresponding 4-arylidene-5-imidazolinones in good yields.
