Cas no 78224-47-2 (Methyl 8-methoxyquinoline-2-carboxylate)
Methyl 8-methoxyquinoline-2-carboxylate Chemical and Physical Properties
Names and Identifiers
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- Methyl 8-methoxyquinoline-2-carboxylate
- SCHEMBL4701058
- A865078
- 78224-47-2
- DTXSID80491356
- SB69535
- YNRMQTUOOLBRHW-UHFFFAOYSA-N
- Methyl8-methoxyquinoline-2-carboxylate
-
- MDL: MFCD19286700
- Inchi: 1S/C12H11NO3/c1-15-10-5-3-4-8-6-7-9(12(14)16-2)13-11(8)10/h3-7H,1-2H3
- InChI Key: YNRMQTUOOLBRHW-UHFFFAOYSA-N
- SMILES: O(C)C1=CC=CC2=CC=C(C(=O)OC)N=C21
Computed Properties
- Exact Mass: 217.07389321g/mol
- Monoisotopic Mass: 217.07389321g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 16
- Rotatable Bond Count: 3
- Complexity: 257
- 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: 2.3
- Topological Polar Surface Area: 48.4?2
Methyl 8-methoxyquinoline-2-carboxylate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A189005706-1g |
Methyl 8-methoxyquinoline-2-carboxylate |
78224-47-2 | 95% | 1g |
$540.00 | 2023-09-01 | |
| Chemenu | CM145165-1g |
Methyl 8-methoxyquinoline-2-carboxylate |
78224-47-2 | 95% | 1g |
$580 | 2021-08-05 | |
| Chemenu | CM145165-1g |
Methyl 8-methoxyquinoline-2-carboxylate |
78224-47-2 | 95% | 1g |
$480 | 2024-07-23 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1742613-1g |
Methyl 8-methoxyquinoline-2-carboxylate |
78224-47-2 | 98% | 1g |
¥5092.00 | 2024-07-28 | |
| Ambeed | A545197-1g |
Methyl 8-methoxyquinoline-2-carboxylate |
78224-47-2 | 95+% | 1g |
$485.0 | 2025-04-16 | |
| Crysdot LLC | CD11057603-1g |
Methyl 8-methoxyquinoline-2-carboxylate |
78224-47-2 | 95+% | 1g |
$614 | 2024-07-18 |
Methyl 8-methoxyquinoline-2-carboxylate Related Literature
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Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
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Dan Yang,Yanping Zhou,Xianhong Rui,Jixin Zhu,Ziyang Lu,Eileen Fong,Qingyu Yan RSC Adv., 2013,3, 14960-14962
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Gang Pan,Yi-jie Bao,Jie Xu,Tao Liu,Cheng Liu,Yan-yan Qiu,Xiao-jing Shi,Hui Yu,Ting-ting Jia,Xia Yuan,Ze-ting Yuan,Yi-jun Cao RSC Adv., 2016,6, 42109-42119
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Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
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Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
Additional information on Methyl 8-methoxyquinoline-2-carboxylate
Methyl 8-Methoxyquinoline-2-Carboxylate: A Comprehensive Overview
Methyl 8-methoxyquinoline-2-carboxylate, also known by its CAS number 78224-47-2, is a compound of significant interest in various fields of chemistry and materials science. This compound belongs to the quinoline derivative family, which has been extensively studied due to its unique electronic properties and potential applications in drug development, optoelectronics, and catalysis. The molecule consists of a quinoline ring with a methoxy group at position 8 and a methyl ester at position 2, making it a versatile building block for further chemical modifications.
The synthesis of methyl 8-methoxyquinoline-2-carboxylate involves a series of well-established organic reactions. Typically, the starting material is quinoline, which undergoes functionalization at specific positions to introduce the methoxy and methyl ester groups. Recent advancements in catalytic methods have enabled more efficient and selective syntheses, reducing the environmental footprint of the production process. These improvements are particularly important as industries increasingly prioritize sustainability and green chemistry principles.
One of the most promising applications of methyl 8-methoxyquinoline-2-carboxylate lies in its use as a precursor for advanced materials. For instance, researchers have explored its role in the development of organic light-emitting diodes (OLEDs) due to its ability to act as an electron transport layer. The compound's unique electronic structure allows for efficient charge transport, which is critical for achieving high luminous efficiency in OLED devices. Recent studies have demonstrated that incorporating methyl 8-methoxyquinoline-2-carboxylate into OLED architectures can significantly enhance device performance, making it a valuable component in next-generation display technologies.
In addition to its role in electronics, methyl 8-methoxyquinoline-2-carboxylate has shown potential in pharmaceutical research. The compound's quinoline backbone is known for its bioactivity, and the introduction of methoxy and methyl ester groups can further modulate its pharmacological properties. For example, studies have indicated that this compound may exhibit anti-inflammatory or antioxidant activities, opening avenues for its use in drug discovery programs. Furthermore, the ease of functionalization at the 8-position allows for the creation of derivatives with tailored biological profiles, expanding its therapeutic potential.
The structural versatility of methyl 8-methoxyquinoline-2-carboxylate also makes it an attractive candidate for catalytic applications. Its ability to coordinate with metal ions renders it useful as a ligand in homogeneous catalysis. Recent research has focused on its application in asymmetric catalysis, where it has been employed to facilitate enantioselective reactions. This capability is particularly valuable in the synthesis of chiral molecules, which are essential components in many pharmaceuticals and agrochemicals.
From an environmental perspective, the synthesis and application of methyl 8-methoxyquinoline-2-carboxylate align with current trends toward greener chemical processes. The use of renewable feedstocks and energy-efficient reaction conditions has been prioritized in recent studies, reducing the ecological impact associated with its production. Moreover, the compound's stability under various operating conditions ensures its suitability for long-term applications without compromising environmental safety.
In conclusion, methyl 8-methoxyquinoline-2-carboxylate is a multifaceted compound with diverse applications across multiple disciplines. Its unique chemical structure enables it to serve as a building block for advanced materials, pharmaceutical agents, and catalysts. As research continues to uncover new functionalities and optimize existing processes, this compound is poised to play an increasingly important role in shaping future innovations across various industries.
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