Cas no 1427501-40-3 (Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate)
Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate Chemical and Physical Properties
Names and Identifiers
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- ETHYL 5-AMINO-4-FLUORO-1-METHYL-1H-IMIDAZOLE-2-CARBOXYLATE
- Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate
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- Inchi: 1S/C7H10FN3O2/c1-3-13-7(12)6-10-4(8)5(9)11(6)2/h3,9H2,1-2H3
- InChI Key: PSHGWLJBCCVUIY-UHFFFAOYSA-N
- SMILES: FC1=C(N)N(C)C(C(=O)OCC)=N1
Computed Properties
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 13
- Rotatable Bond Count: 3
- Complexity: 202
- XLogP3: 0.7
- Topological Polar Surface Area: 70.1
Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A069003737-1g |
Ethyl 5-amino-4-fluoro-1-methyl-1h-imidazole-2-carboxylate |
1427501-40-3 | 95% | 1g |
921.05 USD | 2021-06-01 | |
| Chemenu | CM504058-1g |
Ethyl5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate |
1427501-40-3 | 97% | 1g |
$838 | 2023-01-02 |
Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate Related Literature
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1. An integrated microfluidic 3D tumor system for parallel and high-throughput chemotherapy evaluation?Dan Liu,Rui Hu,Zhongchao Huang,Meilin Sun,Kai Han Analyst, 2020,145, 6447-6455
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Hamid Heydari,Mohammad B. Gholivand New J. Chem., 2017,41, 237-244
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Huiying Xu,Lu Zheng,Yu Zhou,Bang-Ce Ye Analyst, 2021,146, 5542-5549
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Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
Additional information on Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate
Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate (CAS No. 1427501-40-3): A Comprehensive Overview
Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate (CAS No. 1427501-40-3) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This imidazole derivative is characterized by its unique molecular structure, featuring an ethyl ester group, a fluorine substituent, and an amino functional group, making it a versatile intermediate in synthetic chemistry. Researchers and industry professionals are increasingly exploring its potential applications, particularly in drug discovery and crop protection.
The compound's chemical properties include a molecular formula of C7H10FN3O2 and a molecular weight of 187.17 g/mol. Its imidazole core is a common motif in bioactive molecules, contributing to its relevance in medicinal chemistry. The presence of the fluoro substituent enhances its metabolic stability and binding affinity, which is crucial for developing targeted therapies. These attributes make Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate a valuable building block for designing novel compounds.
One of the most searched questions about this compound is: "What are the applications of Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate in drug development?" Recent studies highlight its role as a key intermediate in synthesizing small-molecule inhibitors and kinase modulators, which are pivotal in treating diseases like cancer and inflammatory disorders. Its fluorinated imidazole structure is particularly advantageous for improving drug bioavailability and reducing side effects, aligning with the growing demand for precision medicine.
In the agrochemical sector, Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate is being investigated for its potential in developing next-generation pesticides. The compound's ability to interact with biological targets in pests while minimizing environmental impact resonates with the global push for sustainable farming solutions. This aligns with trending searches such as "eco-friendly agrochemical intermediates" and "fluorinated compounds in agriculture."
From a synthetic chemistry perspective, the compound's ethyl ester group offers flexibility for further derivatization, enabling researchers to tailor its properties for specific applications. This feature is frequently discussed in forums and publications, addressing queries like "How to modify Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate for enhanced activity?" Such discussions underscore its adaptability in customizing molecular frameworks.
The market for imidazole-based compounds is expanding, driven by their utility in pharmaceuticals, agrochemicals, and materials science. Analysts project steady growth for derivatives like Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate, particularly as the demand for fluorinated bioactive molecules rises. This trend is reflected in search terms such as "market trends for fluorinated imidazoles" and "CAS 1427501-40-3 suppliers."
Quality control and regulatory compliance are critical considerations for manufacturers and users of this compound. Ensuring high purity and consistent performance is essential, especially when it serves as an intermediate in sensitive applications. Searches like "analytical methods for Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate" and "CAS 1427501-40-3 specifications" highlight the importance of reliable sourcing and characterization.
In summary, Ethyl 5-amino-4-fluoro-1-methyl-1H-imidazole-2-carboxylate (CAS No. 1427501-40-3) is a multifaceted compound with broad applicability in cutting-edge research and industrial processes. Its unique structural features and functional groups make it a cornerstone in the development of innovative solutions across multiple sectors. As scientific advancements continue, this compound is poised to play an increasingly prominent role in addressing contemporary challenges in health and sustainability.
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