Cas no 29040-48-0 (6-methoxy-2-methyl-Benzofuran)
6-methoxy-2-methyl-Benzofuran Chemical and Physical Properties
Names and Identifiers
-
- 6-methoxy-2-methyl-Benzofuran
- 6-methoxy-2-methyl-1-benzofuran
- 6-Methoxy-2-methylbenzofuran
- 2-Methyl-6-methoxybenzofuran
- 6-methoxy-2-methylbenzo< b> furan
- ACT10776
- AGN-PC-00KGI7
- ANW-64508
- Benzofuran, 6-methoxy-2-methyl-
- CTK0I4885
- SureCN719714
- HS-3057
- 29040-48-0
- SCHEMBL719714
- AHAVOXPDABUPJT-UHFFFAOYSA-N
- 6-methoxy-2methylbenzofuran
- AKOS006311701
- DB-086648
- DTXSID50515174
-
- Inchi: 1S/C10H10O2/c1-7-5-8-3-4-9(11-2)6-10(8)12-7/h3-6H,1-2H3
- InChI Key: AHAVOXPDABUPJT-UHFFFAOYSA-N
- SMILES: O1C(C)=CC2C=CC(=CC1=2)OC
Computed Properties
- Exact Mass: 162.068079557g/mol
- Monoisotopic Mass: 162.068079557g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 12
- Rotatable Bond Count: 1
- Complexity: 158
- 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: 2.7
- Topological Polar Surface Area: 22.4?2
6-methoxy-2-methyl-Benzofuran Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM154488-1g |
6-methoxy-2-methylbenzofuran |
29040-48-0 | 95% | 1g |
$729 | 2021-06-09 | |
| Alichem | A019097070-1g |
6-Methoxy-2-methylbenzofuran |
29040-48-0 | 95% | 1g |
$640.56 | 2023-09-02 | |
| Chemenu | CM154488-1g |
6-methoxy-2-methylbenzofuran |
29040-48-0 | 95% | 1g |
$729 | 2023-02-17 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1732516-1g |
6-Methoxy-2-methylbenzofuran |
29040-48-0 | 98% | 1g |
¥6182.00 | 2024-05-20 |
6-methoxy-2-methyl-Benzofuran Related Literature
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Juan J. Sánchez,Miguel López-Haro,Juan C. Hernández-Garrido,Ginesa Blanco,Miguel A. Cauqui,José M. Rodríguez-Izquierdo,José A. Pérez-Omil,José J. Calvino,María P. Yeste J. Mater. Chem. A, 2019,7, 8993-9003
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Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
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Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
Additional information on 6-methoxy-2-methyl-Benzofuran
Professional Introduction to Compound with CAS No. 29040-48-0 and Product Name: 6-methoxy-2-methyl-Benzofuran
6-methoxy-2-methyl-Benzofuran, identified by the Chemical Abstracts Service Number (CAS No.) 29040-48-0, is a significant organic compound that has garnered considerable attention in the field of pharmaceutical chemistry and natural product synthesis. This benzofuran derivative, characterized by its methoxy and methyl substituents, exhibits a unique structural framework that makes it a valuable intermediate in the development of various bioactive molecules. The compound’s chemical structure, featuring a fused benzene and furan ring system, provides a versatile platform for further functionalization, enabling its application in multiple synthetic pathways.
The benzofuran scaffold is a privileged structure in medicinal chemistry due to its prevalence in numerous pharmacologically active compounds. Its aromatic system allows for easy modification at multiple positions, making it an ideal candidate for designing molecules with specific biological activities. The presence of both 6-methoxy and 2-methyl groups in 6-methoxy-2-methyl-Benzofuran enhances its reactivity and contributes to its potential as a precursor in drug discovery programs. These substituents not only influence the electronic properties of the molecule but also play a crucial role in determining its interaction with biological targets.
In recent years, there has been growing interest in exploring the pharmacological potential of benzofuran derivatives. Studies have demonstrated that modifications within the benzofuran core can lead to compounds with diverse biological effects, including anti-inflammatory, antimicrobial, and anticancer properties. The 6-methoxy-2-methyl configuration of this compound has been particularly studied for its ability to modulate certain enzyme activities and receptor interactions. For instance, research has indicated that derivatives of this nature may exhibit inhibitory effects on enzymes such as cyclooxygenase (COX) and lipoxygenase (LOX), which are implicated in inflammatory processes.
One of the most compelling aspects of 6-methoxy-2-methyl-Benzofuran is its utility as a building block in synthetic chemistry. The benzofuran ring system can be further functionalized through various chemical reactions, such as hydroxylation, methylation, or coupling with other heterocyclic structures. This flexibility allows chemists to tailor the compound???s properties to meet specific requirements for drug development. Additionally, the methoxy group provides a site for electrophilic aromatic substitution reactions, enabling the introduction of additional functional groups that can enhance binding affinity to biological targets.
Recent advancements in computational chemistry have also contributed to the understanding of 6-methoxy-2-methyl-Benzofuran’s potential applications. Molecular modeling studies have been employed to predict how this compound might interact with various biological targets, providing insights into its mechanism of action. These simulations have helped researchers identify key binding pockets and optimize the structure for improved efficacy. Furthermore, the use of high-throughput screening techniques has facilitated the rapid identification of analogs with enhanced biological activity, further solidifying the importance of benzofuran derivatives in drug discovery.
The synthesis of 6-methoxy-2-methyl-Benzofuran itself is an intriguing process that highlights the ingenuity of organic chemists. Traditional synthetic routes often involve multi-step sequences starting from readily available precursors such as coumarin or diarylalkanes. Modern synthetic methodologies have improved efficiency and yield, making it possible to produce this compound on a larger scale for industrial applications. Catalytic processes, including transition metal-catalyzed cross-coupling reactions, have been particularly effective in constructing the benzofuran core with high precision.
The pharmaceutical industry has taken notice of the synthetic versatility and biological potential of 6-methoxy-2-methyl-Benzofuran. Several companies are currently exploring derivatives of this compound as leads for new therapeutic agents. Preclinical studies have shown promising results in models of inflammation and cancer, suggesting that further development could yield novel drugs with significant clinical benefits. The compound’s ability to cross biological membranes also makes it an attractive candidate for oral administration, which could enhance patient compliance compared to injectable therapies.
From a natural product perspective, 6-methoxy-2-methyl-Benzofuran can be found in certain plant species, where it likely contributes to their defensive mechanisms against herbivores or pathogens. The presence of this compound in nature underscores its biological relevance and reinforces its importance as a starting point for synthetic chemists. By studying how plants biosynthesize benzofurans, researchers can gain insights into potential new synthetic strategies and discover additional bioactive molecules within these natural scaffolds.
The environmental impact of producing and utilizing 6-methoxy-2-methyl-Benzofuran is another consideration that merits discussion. While the compound itself is not classified as hazardous or toxic under normal conditions, sustainable practices should be employed during its synthesis and application to minimize environmental footprint. Green chemistry principles encourage the use of renewable feedstocks, efficient catalytic systems, and solvent-free reactions where possible. By adopting these approaches, manufacturers can ensure that their production processes align with global efforts to promote sustainability.
In conclusion,6-methoxy-2-methyl-Benzofuran (CAS No. 29040-48-0) represents a fascinating compound with broad applications in pharmaceutical research and industrial chemistry. Its unique structural features make it a valuable intermediate for synthesizing bioactive molecules with potential therapeutic uses. As research continues to uncover new derivatives and applications,benzofuran-based compounds like this one will undoubtedly play an increasingly important role in addressing global health challenges.
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