791569-71-6 Usage
Uses
Used in Pharmaceutical Development:
1H-Imidazole-2-acetic acid, ethyl ester (9CI) is used as a pharmaceutical intermediate for the synthesis of various medications. Its unique chemical properties and physiological activity make it a valuable component in the development of new drugs.
Used in Organic Synthesis:
1H-Imidazole-2-acetic acid, ethyl ester (9CI) is used as a reagent in organic synthesis processes. Its nucleophilic nature and ethyl ester group contribute to the formation of complex organic molecules, which can be utilized in various applications.
Used in Biological Materials:
1H-Imidazole-2-acetic acid, ethyl ester (9CI) is used as a component in the development of biological materials. Its solubility and membrane permeability enhance its potential for use in creating materials with specific biological properties or functions.
Check Digit Verification of cas no
The CAS Registry Mumber 791569-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,5,6 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 791569-71:
(8*7)+(7*9)+(6*1)+(5*5)+(4*6)+(3*9)+(2*7)+(1*1)=216
216 % 10 = 6
So 791569-71-6 is a valid CAS Registry Number.
791569-71-6Relevant articles and documents
A switching cascade of hydrazone-based rotary switches through coordination-coupled proton relays
Ray, Debdas,Foy, Justin T.,Hughes, Russell P.,Aprahamian, Ivan
, p. 757 - 762 (2012)
Imidazole, a subunit of histidine, plays a crucial role in proton-relay processes that are important for various biological activities, such as metal efflux, viral replication and photosynthesis. We show here how an imidazolyl ring incorporated into a rotary switch based on a hydrazone enables a switching cascade that involves proton relay between two different switches. The switching process starts with a single input, zinc(II), that initiates an E/Z isomerization in the hydrazone system through a coordination-coupled proton transfer. The resulting imidazolium ring is unusually acidic and, through proton relay, activates the E/Z isomerization of a non-coordinating pyridine-containing hydrazone switch. We hypothesize that the reduction in the acid dissociation constant of the imidazolium ring results from a combination of electrostatic and conformational effects, the study of which might help elucidate the proton-coupled electron-transfer mechanism in photosynthetic bacteria.
