1203852-75-8 Usage
Description
1-(2-(methoxycarbonyl)-4-nitrophenyl)-5-methyl-1H-imidazole-4-carboxylic acid ethyl ester is a complex chemical compound that is an ester derivative of an imidazole carboxylic acid. It features a methoxycarbonyl and nitrophenyl group attached to the imidazole ring, along with an ethyl ester group. This unique aromatic and heterocyclic structure suggests potential applications in pharmaceuticals, organic synthesis, and materials science. Its biological properties may also contribute to its utility in drug discovery and medicinal chemistry.
Uses
Used in Pharmaceutical Applications:
1-(2-(methoxycarbonyl)-4-nitrophenyl)-5-methyl-1H-imidazole-4-carboxylic acid ethyl ester is used as a pharmaceutical compound for its potential therapeutic properties. Its unique structure may allow it to interact with various biological targets, making it a candidate for the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(2-(methoxycarbonyl)-4-nitrophenyl)-5-methyl-1H-imidazole-4-carboxylic acid ethyl ester is used as a synthetic building block. Its versatile structure can be modified to create a variety of new compounds with different properties and applications.
Used in Materials Science:
1-(2-(methoxycarbonyl)-4-nitrophenyl)-5-methyl-1H-imidazole-4-carboxylic acid ethyl ester is used as a component in the development of new materials. Its aromatic and heterocyclic structure may contribute to the creation of materials with unique properties, such as improved stability or enhanced functionality.
Used in Research and Development:
In the field of research and development, 1-(2-(methoxycarbonyl)-4-nitrophenyl)-5-methyl-1H-imidazole-4-carboxylic acid ethyl ester is used as a chemical probe. Its diverse applications and potential biological properties make it a valuable tool for exploring new avenues in drug discovery and medicinal chemistry.
Overall, 1-(2-(methoxycarbonyl)-4-nitrophenyl)-5-methyl-1H-imidazole-4-carboxylic acid ethyl ester is a versatile compound with a wide range of potential applications across various industries. Its unique structure and properties make it an interesting candidate for further research and development in pharmaceuticals, organic synthesis, materials science, and other related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1203852-75-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,3,8,5 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1203852-75:
(9*1)+(8*2)+(7*0)+(6*3)+(5*8)+(4*5)+(3*2)+(2*7)+(1*5)=128
128 % 10 = 8
So 1203852-75-8 is a valid CAS Registry Number.
1203852-75-8Relevant articles and documents
A concise and efficient synthesis of flumazenil and its precursor for radiolabeling with fluorine-18
Donohue, Sean R.,Dannals, Robert F.
supporting information; experimental part, p. 7271 - 7273 (2010/03/03)
Presently there is a strong interest in developing radioligands for in vivo imaging the GABAA-Bz site with positron emission tomography (PET). Flumazenil (1), a high-affinity GABAA-Bz site inverse agonist, is amenable for 11C and 18F-labeling. The current methods for synthesis of 1 and its precursor for 18F-labeling are not ideal and restrict structure-activity relationship (SAR) development. Herein we present a novel and less troublesome synthesis of 1 and its cognates to aid in the development of improved radioligands for PET imaging of GABAA-Bz site.
