117296-92-1 Usage
Description
Ethyl 2-(1H-imidazol-1-yl)benzoate, with the molecular formula C11H12N2O2, is a chemical compound that belongs to the class of phenylmethylimidazoles. It features a phenyl group attached to an imidazole ring and a benzoate ester group, which gives it unique structural properties that make it valuable in various areas of chemistry. However, its precise usage, safety data, potential hazards, and environmental impact require extensive research and careful handling.
Uses
Used in Chemical Research:
Ethyl 2-(1H-imidazol-1-yl)benzoate is used as a research compound for studying its chemical properties and potential applications in various fields. Its unique structure allows for exploration in areas such as pharmaceuticals, materials science, and catalysis.
Used in Pharmaceutical Development:
Ethyl 2-(1H-imidazol-1-yl)benzoate is used as a building block or intermediate in the synthesis of pharmaceutical compounds. Its imidazole and benzoate groups can be utilized in the development of new drugs with potential therapeutic applications.
Used in Material Science:
Ethyl 2-(1H-imidazol-1-yl)benzoate is used as a component in the development of new materials with specific properties, such as conductivity, stability, or reactivity. Its structural features can contribute to the creation of advanced materials for various applications.
Used in Catalyst Design:
Ethyl 2-(1H-imidazol-1-yl)benzoate is used as a catalyst or catalyst precursor in chemical reactions. Its imidazole and benzoate groups can facilitate or enhance the rate of certain reactions, making it a valuable tool in the field of catalysis.
Check Digit Verification of cas no
The CAS Registry Mumber 117296-92-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,2,9 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 117296-92:
(8*1)+(7*1)+(6*7)+(5*2)+(4*9)+(3*6)+(2*9)+(1*2)=141
141 % 10 = 1
So 117296-92-1 is a valid CAS Registry Number.
117296-92-1Relevant articles and documents
Aromatic hydrazides as specific inhibitors of bovine serum amine oxidase
Artico,Silvestri,Stefancich,Avigliano,Di Giulio,Maccarrone,Agostinelli,Mondovi,Morpurgo
, p. 219 - 228 (2007/10/02)
New hydrazides were synthesized in search for specific inhibitors of bovine serum amine oxidase: a series of benzoic and phenylacetic acid hydrazides containing the 1H-imidazol-1-yl or the 1H-imidazol-1-ylmethyl group as (o,m,p)-substituent in the phenyl ring; an analogous series of p-substituted phenylhydrazides with 5 or 6-membered heterocyclic ring as substituent, and a series of similar phenylpropionic hydrazides. The longer and more flexible phenylacetic hydrazides, and to a somewhat lesser extent the phenylpropionic ones, were better specific inhibitors of bovine serum amine oxidase than the benzoic hydrazides, which were also bound by the enzyme with high affinity, but at a slow rate. Derivatives with p- and m-substituents were more reactive than the o-substituted ones. The chemical nature of the substituent was less important than its position in the phenyl ring and the presence of methylene spacers. These data point to the presence of a hydrophobic site at short distance from the protein carbonyl cofactor, so that simultaneous interaction of the 2 ends of the inhibitor molecule can occur at the 2 sites. The presence of the hydrophobic site was confirmed by the capability of some molecule deprived of the hydrazidic group to act as mild inhibitors. All hydrazides were less reactive by 2-3 orders of magnitude towards pig kidney diamine oxidase and FAD-dependent monoamine oxidase from rat brain mitochondria, while the other compounds showed similar inhibition power against all proteins. The specificity for the bovine enzyme seems therefore to be related to the concerted action of the 2 moieties of the inhibitor molecule.
