25023-22-7 Usage
Description
IMIDAZOL-1-YL-ACETIC ACID METHYL ESTER is a chemical compound characterized by the molecular formula C6H8N2O2. It is a methyl ester derivative of imidazole-1-ylacetic acid, featuring both an imidazole ring and a carboxylic acid group. This versatile compound is recognized for its potential biological and pharmacological activities, establishing it as a significant precursor in the synthesis of pharmaceuticals and organic compounds. Its valuable role in drug development and medicinal chemistry is attributed to its wide range of applications across various research and industrial domains.
Uses
Used in Pharmaceutical Synthesis:
IMIDAZOL-1-YL-ACETIC ACID METHYL ESTER serves as a key precursor in the pharmaceutical industry, utilized for the synthesis of various drugs. Its unique structure allows for the development of compounds with specific biological activities, contributing to the creation of novel therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, IMIDAZOL-1-YL-ACETIC ACID METHYL ESTER is employed as a building block for designing and optimizing new molecules with desired pharmacological properties. Its presence in the molecular structure can influence the compound's interaction with biological targets, enhancing the effectiveness of potential drugs.
Used in Organic Chemistry Research:
IMIDAZOL-1-YL-ACETIC ACID METHYL ESTER is also widely used in organic chemistry research for studying reaction mechanisms and exploring new synthetic pathways. Its reactivity and functional groups make it a suitable candidate for various organic transformations, broadening the scope of chemical research.
Used in Chemical Industry:
The chemical industry leverages IMIDAZOL-1-YL-ACETIC ACID METHYL ESTER for the production of various organic compounds and intermediates. Its versatility and compatibility with different chemical processes make it a valuable component in the synthesis of specialty chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 25023-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,2 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25023-22:
(7*2)+(6*5)+(5*0)+(4*2)+(3*3)+(2*2)+(1*2)=67
67 % 10 = 7
So 25023-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2O2/c1-10-6(9)4-8-3-2-7-5-8/h2-3,5H,4H2,1H3
25023-22-7Relevant articles and documents
Hydroxyethyl and ester co-functionalized imidazolium iodide for highly efficient solid-state dye-sensitized solar cells
Li, Juan,Wang, Hong,Zhou, Gang,Wang, Zhong-Sheng
, p. 9446 - 9448 (2013)
Hydroxyethyl and ester co-functionalized imidazolium iodide has been designed and synthesized as an efficient solid state electrolyte for dye-sensitized solar cells. Single crystal X-ray analyses confirm the presence of ordered three dimensional ionic channels for iodide, which exhibits high conductivity when mixed with iodine and LiI and achieves a power conversion efficiency of 7.45%.
POSS with eight imidazolium iodide arms for efficient solid-state dye-sensitized solar cells
Zhang, Wei,Li, Juan,Jiang, Shenghui,Wang, Zhong-Sheng
supporting information, p. 1685 - 1687 (2014/02/14)
Polyhedral oligomeric silsesquioxane functionalized with eight imidazolium iodide arms has been designed and synthesized for use as solid-state electrolytes in solid-state dye-sensitized solar cells, which exhibits a power conversion efficiency of 7.11% under one sun illumination and good long-term stability under one sun soaking.
Development of imidazole alkanoic acids as mGAT3 selective GABA uptake inhibitors
Hack, Silke,W?rlein, Babette,H?fner, Georg,Pabel, J?rg,Wanner, Klaus T.
experimental part, p. 1483 - 1498 (2011/05/11)
A new series of potential GABA uptake inhibitors starting from of 1H-imidazol-4-ylacetic acid with the carboxylic acid side chain originating from different positions and varying in length have been synthesized and tested for the inhibitory potency at the