78892-68-9 Usage
Uses
Used in Organic Synthesis:
1H-Imidazole-4-carboxylic acid, 5-methyl-, methyl ester (9CI) is used as a synthetic intermediate for the preparation of various organic compounds. Its unique imidazole ring structure allows it to participate in a range of chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1H-Imidazole-4-carboxylic acid, 5-methyl-, methyl ester (9CI) is used as a key building block in the development of new drugs and bioactive compounds. Its potential to form stable complexes with biological targets makes it a promising candidate for the creation of novel therapeutic agents.
Used in Material Science:
1H-Imidazole-4-carboxylic acid, 5-methyl-, methyl ester (9CI) may also find applications in material science, where it can be employed as a component in the design and synthesis of advanced materials with specific properties. Its ability to form stable structures and interact with other molecules makes it a candidate for use in the development of new materials with tailored characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 78892-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,9 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78892-68:
(7*7)+(6*8)+(5*8)+(4*9)+(3*2)+(2*6)+(1*8)=199
199 % 10 = 9
So 78892-68-9 is a valid CAS Registry Number.
78892-68-9Relevant academic research and scientific papers
Design and synthesis of novel potent antinociceptive agents: Methyl-imidazolyl N-acylhydrazone derivatives
Figueiredo, Juliana M.,Camara, Celso De A.,Amarante, Emanuel G.,Miranda, Ana Luisa P.,Santos, Fulvia M.,Rodrigues, Carlos R.,Fraga, Carlos Alberto M.,Barreiro, Eliezer J.
, p. 2243 - 2248 (2007/10/03)
This paper describes recent results of design, synthesis and pharmacological evaluation of new N-heterocyclic functionalized N-acylhydrazone compounds, belonging to the 2-methyl-imidazolyl-3-acylhydrazone class (4a-e). These compounds were planned by applying the molecular simplification strategy to propose the structural modifications on the previously described functionalized imidazo[1,2-a]pyridine 3-acylhydrazone series (2), which presented an important analgesic profile. This new series (4) was synthesized in order to investigate the possible pharmacophoric contribution of the N-heteroaromatic ring and N-acylhydrazone moieties to the analgesic activity. Compounds 4a-b are the most potent antinociceptive agents from this series. Copyright (C) 2000 Elsevier Science Ltd.
Process for preparing 5-methyl-4-imidazolecarboxylic acid esters
-
, (2008/06/13)
A process for the preparation of 5-methyl-4-imidazolecarboxylic acid esters from acetoacetic acid esters. The products of this process are useful as intermediates for preparing cimetidine.
