Cas no 99968-74-8 (5-methylfuran-2-carboxamide)
5-methylfuran-2-carboxamide Chemical and Physical Properties
Names and Identifiers
-
- 2-Furancarboxamide,5-methyl-
- 2-Furancarboxamide,5-methyl-(9CI)
- 5-Methylfuran-2-carboxamide
- DTXSID70409081
- SCHEMBL279424
- AKOS003884763
- HTLIXYXARPLOIU-UHFFFAOYSA-N
- EN300-173695
- BS-51063
- Z33547151
- E78248
- 5-Methyl-2-furamide
- 5-METHYL-2-FURANCARBOXAMIDE
- 99968-74-8
- STK358677
- 2-Furancarboxamide, 5-methyl-
- DB-281544
- 5-methylfuran-2-carboxamide
-
- Inchi: 1S/C6H7NO2/c1-4-2-3-5(9-4)6(7)8/h2-3H,1H3,(H2,7,8)
- InChI Key: HTLIXYXARPLOIU-UHFFFAOYSA-N
- SMILES: O1C(C(N)=O)=CC=C1C
Computed Properties
- Exact Mass: 125.047678466g/mol
- Monoisotopic Mass: 125.047678466g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 9
- Rotatable Bond Count: 1
- Complexity: 124
- 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: 0.6
- Topological Polar Surface Area: 56.2?2
5-methylfuran-2-carboxamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | M328045-25mg |
5-methylfuran-2-carboxamide |
99968-74-8 | 25mg |
$ 50.00 | 2022-06-04 | ||
| TRC | M328045-50mg |
5-methylfuran-2-carboxamide |
99968-74-8 | 50mg |
$ 70.00 | 2022-06-04 | ||
| TRC | M328045-250mg |
5-methylfuran-2-carboxamide |
99968-74-8 | 250mg |
$ 295.00 | 2022-06-04 | ||
| Chemenu | CM531301-250mg |
5-Methylfuran-2-carboxamide |
99968-74-8 | 97% | 250mg |
$*** | 2023-04-18 | |
| Chemenu | CM531301-1g |
5-Methylfuran-2-carboxamide |
99968-74-8 | 97% | 1g |
$*** | 2023-04-18 | |
| Enamine | EN300-173695-1g |
5-methylfuran-2-carboxamide |
99968-74-8 | 95% | 1g |
$355.0 | 2023-09-20 | |
| Enamine | EN300-173695-5g |
5-methylfuran-2-carboxamide |
99968-74-8 | 95% | 5g |
$1033.0 | 2023-09-20 | |
| Enamine | EN300-173695-10g |
5-methylfuran-2-carboxamide |
99968-74-8 | 95% | 10g |
$1531.0 | 2023-09-20 | |
| eNovation Chemicals LLC | Y1226615-1g |
5-Methylfuran-2-carboxamide |
99968-74-8 | 95% | 1g |
$300 | 2024-06-03 | |
| Enamine | EN300-173695-0.05g |
5-methylfuran-2-carboxamide |
99968-74-8 | 95% | 0.05g |
$65.0 | 2023-09-20 |
5-methylfuran-2-carboxamide Related Literature
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Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
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Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
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Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
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Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
Additional information on 5-methylfuran-2-carboxamide
Introduction to 5-methylfuran-2-carboxamide (CAS No. 99968-74-8)
5-methylfuran-2-carboxamide is a significant compound in the realm of organic chemistry and pharmaceutical research, characterized by its unique structural and functional properties. This compound, identified by the Chemical Abstracts Service Number (CAS No.) 99968-74-8, has garnered attention due to its potential applications in the synthesis of bioactive molecules and its role in advancing chemical biology studies. The molecular structure of 5-methylfuran-2-carboxamide consists of a furan ring substituted with a methyl group at the 5-position and an amide functional group at the 2-position, which contributes to its reactivity and versatility in synthetic chemistry.
The 5-methylfuran-2-carboxamide molecule exhibits notable characteristics that make it a valuable intermediate in the pharmaceutical industry. Its ability to participate in various chemical transformations, such as nucleophilic addition and condensation reactions, allows for the facile synthesis of more complex molecules. These properties have been leveraged in recent research to develop novel therapeutic agents targeting various biological pathways. The compound’s stability under different conditions and its compatibility with a range of solvents further enhance its utility in laboratory settings.
In recent years, the study of 5-methylfuran-2-carboxamide has been integrated into broader research initiatives aimed at discovering new pharmacophores and developing innovative drug candidates. One particularly intriguing area of investigation involves its use as a precursor in the synthesis of bioactive peptides and proteins. The amide group in 5-methylfuran-2-carboxamide provides a scaffold for introducing specific amino acid residues, enabling the creation of peptidomimetics with enhanced stability and bioavailability. Such modifications are crucial for developing next-generation drugs that can overcome limitations associated with traditional peptide-based therapies.
Moreover, the structural motif of 5-methylfuran-2-carboxamide has been explored in the context of medicinal chemistry for its potential to interact with biological targets. Researchers have identified that the furan ring can engage with specific binding pockets in enzymes and receptors, modulating their activity. This insight has led to the design of 5-methylfuran-2-carboxamide derivatives as inhibitors or activators of key metabolic pathways. For instance, studies have demonstrated that certain analogs exhibit inhibitory effects on enzymes involved in inflammation and oxidative stress, suggesting their therapeutic potential in managing chronic diseases.
The synthesis of 5-methylfuran-2-carboxamide itself is another area where advancements have been made. Modern synthetic methodologies have enabled more efficient and scalable production processes, reducing costs and improving yields. These developments are particularly important for industrial applications where large quantities of high-purity material are required. Additionally, green chemistry principles have been incorporated into synthetic routes for 5-methylfuran-2-carboxamide, minimizing waste and utilizing environmentally friendly reagents. Such approaches align with global efforts to promote sustainable chemical manufacturing.
Recent computational studies have also shed light on the electronic properties of 5-methylfuran-2-carboxamide, providing insights into its reactivity and interaction with other molecules. Through molecular modeling techniques, researchers have been able to predict how this compound might behave in different environments, aiding in the rational design of experiments. These computational tools are indispensable in modern drug discovery, allowing scientists to screen vast libraries of compounds efficiently before conducting costly wet-lab experiments.
The applications of 5-methylfuran-2-carboxamide extend beyond pharmaceuticals into materials science and agrochemicals. Its unique structural features make it a promising candidate for developing novel polymers with enhanced mechanical properties or for use as a chiral auxiliary in asymmetric synthesis. In agrochemical research, derivatives of 5-methylfuran-2-carboxamide have shown potential as intermediates for synthesizing pesticides and herbicides that are more effective and environmentally benign.
As our understanding of chemical biology evolves, the role of compounds like 5-methylfuran-2-carboxamide is expected to grow even further. Ongoing research is exploring new ways to harness its potential, from developing innovative synthetic strategies to uncovering novel biological functions. The collaborative efforts between chemists, biologists, and pharmacologists are driving these advancements forward, paving the way for breakthroughs that could revolutionize medicine and industry.
In conclusion, 5-methylfuran-2-carboxamide (CAS No. 99968-74-8) represents a compound of considerable interest due to its versatile applications and structural features. Its significance in pharmaceutical research, particularly in the development of bioactive molecules and drug candidates, underscores its importance as a chemical building block. As scientific understanding progresses, it is likely that new applications for this compound will continue to emerge, reinforcing its position as a cornerstone in modern chemical innovation.
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