92809-78-4 Usage
Structure
1H-Imidazole-4-carboxylic acid with a phenyl group attached to the 5-position and an ethyl ester group
Type
Ethyl ester of 1H-imidazole-4-carboxylic acid
Applications
Potential use in medicinal chemistry and pharmaceutical research, as imidazole derivatives are known for their biological activities and pharmacological properties
Suitability
As a reagent in organic synthesis and drug development, and for studying the structure-activity relationships of imidazole-based compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 92809-78-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,0 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 92809-78:
(7*9)+(6*2)+(5*8)+(4*0)+(3*9)+(2*7)+(1*8)=164
164 % 10 = 4
So 92809-78-4 is a valid CAS Registry Number.
92809-78-4Relevant academic research and scientific papers
PHOTOCHEMICAL WOLFF REARRANGEMENT OF 5-DIAZO-6-PHENYLURACIL IN NEUTRAL SOLUTIONS. THE SYNTHESIS OF ALKYL 5-PHENYL-2-OXO-4-IMIDAZOLINE-4-CARBOXYLIC ACID DERIVATIVES
Kloetzer, Wilhelm,Doerler, Gerhard,Stanovnik, Branko,Tisler, Miha
, p. 1763 - 1769 (2007/10/02)
A photochemical Wolff rearrangement of 5-diazo-6-phenyluracil (6), the compound which does not form the corresponding hydrate or alcohol adducts, into alkyl 5-phenyl-2-oxo-4-imidazoline-4-carboxylic acid derivatives 8a-h in neutral solutions is described.
