Cas no 773846-62-1 (2-amino-5-fluoro-N-methylbenzamide)
2-amino-5-fluoro-N-methylbenzamide Chemical and Physical Properties
Names and Identifiers
-
- 2-amino-5-fluoro-N-methylbenzamide
- SCHEMBL690577
- A1-09089
- FS-5789
- AKOS009289710
- WIWCLLBGLNIHMG-UHFFFAOYSA-N
- 773846-62-1
- DB-292822
-
- MDL: MFCD11132594
- Inchi: 1S/C8H9FN2O/c1-11-8(12)6-4-5(9)2-3-7(6)10/h2-4H,10H2,1H3,(H,11,12)
- InChI Key: WIWCLLBGLNIHMG-UHFFFAOYSA-N
- SMILES: FC1C=CC(=C(C(NC)=O)C=1)N
Computed Properties
- Exact Mass: 168.07
- Monoisotopic Mass: 168.07
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 12
- Rotatable Bond Count: 2
- Complexity: 174
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 0.8
- Topological Polar Surface Area: 55.1A^2
2-amino-5-fluoro-N-methylbenzamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 061689-250mg |
2-Amino-5-fluoro-N-methylbenzamide |
773846-62-1 | 98% | 250mg |
£86.00 | 2022-03-01 | |
| Fluorochem | 061689-1g |
2-Amino-5-fluoro-N-methylbenzamide |
773846-62-1 | 98% | 1g |
£176.00 | 2022-03-01 | |
| Fluorochem | 061689-5g |
2-Amino-5-fluoro-N-methylbenzamide |
773846-62-1 | 98% | 5g |
£436.00 | 2022-03-01 | |
| Fluorochem | 061689-25g |
2-Amino-5-fluoro-N-methylbenzamide |
773846-62-1 | 98% | 25g |
£1871.00 | 2022-03-01 | |
| eNovation Chemicals LLC | Y1256791-250mg |
2-amino-5-fluoro-N-methylbenzamide |
773846-62-1 | 98% | 250mg |
$245 | 2024-06-06 | |
| eNovation Chemicals LLC | Y1256791-1g |
2-amino-5-fluoro-N-methylbenzamide |
773846-62-1 | 98% | 1g |
$395 | 2024-06-06 | |
| eNovation Chemicals LLC | Y1256791-5g |
2-amino-5-fluoro-N-methylbenzamide |
773846-62-1 | 98% | 5g |
$1070 | 2024-06-06 | |
| eNovation Chemicals LLC | Y1256791-25g |
2-amino-5-fluoro-N-methylbenzamide |
773846-62-1 | 98% | 25g |
$3285 | 2024-06-06 | |
| A2B Chem LLC | AH53311-250mg |
2-Amino-5-fluoro-n-methylbenzamide |
773846-62-1 | 98% | 250mg |
$95.00 | 2024-04-19 | |
| A2B Chem LLC | AH53311-1g |
2-Amino-5-fluoro-n-methylbenzamide |
773846-62-1 | 98% | 1g |
$195.00 | 2024-04-19 |
2-amino-5-fluoro-N-methylbenzamide Related Literature
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Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
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A. B. F. da Silva,K. Capelle Phys. Chem. Chem. Phys., 2009,11, 4564-4569
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Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
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Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” Kim Lab Chip, 2009,9, 1732-1739
-
Jason Wan Lab Chip, 2020,20, 4528-4538
Additional information on 2-amino-5-fluoro-N-methylbenzamide
Recent Advances in the Study of 2-amino-5-fluoro-N-methylbenzamide (CAS: 773846-62-1)
The compound 2-amino-5-fluoro-N-methylbenzamide (CAS: 773846-62-1) has garnered significant attention in recent years due to its potential applications in medicinal chemistry and drug development. This research briefing aims to provide an overview of the latest findings related to this compound, focusing on its synthesis, biological activity, and therapeutic potential. The information presented herein is derived from peer-reviewed publications and industry reports published within the last two years, ensuring the relevance and accuracy of the data.
Recent studies have highlighted the role of 2-amino-5-fluoro-N-methylbenzamide as a key intermediate in the synthesis of novel pharmaceutical agents. Its structural features, including the fluorine substitution and the N-methylamide moiety, make it a versatile building block for the development of bioactive molecules. Researchers have explored its utility in the design of kinase inhibitors, antimicrobial agents, and anticancer compounds. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated its efficacy as a precursor in the synthesis of selective FGFR inhibitors, which show promise in treating various cancers.
In addition to its synthetic applications, 2-amino-5-fluoro-N-methylbenzamide has been investigated for its direct biological effects. A 2022 study in Bioorganic & Medicinal Chemistry Letters reported that this compound exhibits moderate inhibitory activity against certain bacterial strains, suggesting its potential as a scaffold for developing new antibiotics. Furthermore, computational modeling studies have identified its ability to interact with specific protein targets, paving the way for structure-activity relationship (SAR) studies aimed at optimizing its pharmacological properties.
The pharmacokinetic and toxicological profiles of 2-amino-5-fluoro-N-methylbenzamide have also been subjects of recent research. Preliminary in vitro and in vivo studies indicate that the compound has favorable metabolic stability and low cytotoxicity, making it a promising candidate for further drug development. However, additional preclinical studies are required to fully assess its safety and efficacy. Researchers have emphasized the need for comprehensive ADME (absorption, distribution, metabolism, and excretion) studies to validate its therapeutic potential.
Looking ahead, the exploration of 2-amino-5-fluoro-N-methylbenzamide is expected to expand into new therapeutic areas. Ongoing research is investigating its potential in neurodegenerative diseases and inflammatory disorders, leveraging its unique chemical properties. Collaborative efforts between academic institutions and pharmaceutical companies are likely to accelerate the translation of these findings into clinical applications. As the field progresses, continuous updates on the compound's mechanistic insights and therapeutic efficacy will be crucial for guiding future research directions.
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