Cas no 147623-18-5 (1-(2-methoxy-3,5-dimethylphenyl)ethanone)
1-(2-methoxy-3,5-dimethylphenyl)ethanone Chemical and Physical Properties
Names and Identifiers
-
- 1-(2-methoxy-3,5-dimethylphenyl)ethanone
- 2-methoxy-3,4-dimethylacetophenone
- AC1MBYGQ
- 3,5-Dimethyl-2-methoxyacetophenone
- SureCN8431119
- 1-(2-methoxy-3,4-dimethyl-phenyl)-ethanone
- 2-Methoxy-3,4-dimethyl-acetophenon
- 3,4-dimethyl-2-methoxyacetophenone
- 1-(2-methoxy-3,4-dimethylphenyl)ethanone
- 1-(2-Methoxy-3,4-dimethyl-phenyl)-aethanon
- SCHEMBL8431119
- 147623-18-5
- DTXSID30933170
- 55169-98-7
- AKOS006278379
- FS-1586
- CS-0363357
- 2'-methoxy-3',5'-dimethylacetophenone
- 1-(2-methoxy-3,5-dimethylphenyl)ethan-1-one
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- Inchi： 1S/C11H14O2/c1-7-5-8(2)11(13-4)10(6-7)9(3)12/h5-6H,1-4H3
- InChI Key： DWERFCCYBUXHNJ-UHFFFAOYSA-N
- SMILES： O(C)C1C(C(C)=O)=CC(C)=CC=1C
Computed Properties
- Exact Mass: 178.09900
- Monoisotopic Mass: 178.099379685g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 13
- Rotatable Bond Count: 2
- Complexity: 189
- 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: 26.3?2
Experimental Properties
- PSA: 26.30000
- LogP: 2.51460
1-(2-methoxy-3,5-dimethylphenyl)ethanone Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A010007625-250mg |
3',4'-Dimethyl-2'-methoxyacetophenone |
147623-18-5 | 97% | 250mg |
480.00 USD | 2021-07-06 | |
| Alichem | A010007625-500mg |
3',4'-Dimethyl-2'-methoxyacetophenone |
147623-18-5 | 97% | 500mg |
823.15 USD | 2021-07-06 | |
| Alichem | A010007625-1g |
3',4'-Dimethyl-2'-methoxyacetophenone |
147623-18-5 | 97% | 1g |
1,564.50 USD | 2021-07-06 |
1-(2-methoxy-3,5-dimethylphenyl)ethanone Related Literature
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Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
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Huiying Xu,Lu Zheng,Yu Zhou,Bang-Ce Ye Analyst, 2021,146, 5542-5549
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Yang Xu,Min Wang,Donghui Wei,Rongqiang Tian,Zheng Duan,Fran?ois Mathey Dalton Trans., 2019,48, 5523-5526
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Jingquan Liu,Huiyun Liu,Zhongfan Jia,Volga Bulmus,Thomas P. Davis Chem. Commun., 2008, 6582-6584
-
Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
Additional information on 1-(2-methoxy-3,5-dimethylphenyl)ethanone
Introduction to 1-(2-Methoxy-3,5-Dimethylphenyl)Ethanone (CAS No. 147623-18-5)
1-(2-Methoxy-3,5-Dimethylphenyl)Ethanone, also known by its CAS registry number 147623-18-5, is a versatile organic compound with significant applications in various fields. This compound belongs to the class of aromatic ketones, characterized by its unique structure that combines a methoxy group and two methyl groups attached to a phenyl ring, which is further connected to an ethanone moiety. The compound's structure not only imparts it with distinct chemical properties but also makes it a valuable molecule in both academic research and industrial applications.
The synthesis of 1-(2-Methoxy-3,5-Dimethylphenyl)Ethanone typically involves multi-step organic reactions, often utilizing Friedel-Crafts acylation or other electrophilic substitution methods. Recent advancements in catalytic systems and green chemistry have enabled more efficient and environmentally friendly routes for its production. For instance, researchers have explored the use of solid acid catalysts to facilitate the acylation step, reducing the need for hazardous solvents and improving overall yields.
One of the most notable applications of 1-(2-Methoxy-3,5-Dimethylphenyl)Ethanone is in the fragrance industry. Its pleasant aroma profile makes it a popular ingredient in perfumes, cosmetics, and personal care products. The compound's stability under various environmental conditions ensures that it retains its fragrance properties over extended periods. Moreover, its ability to blend seamlessly with other aromatic compounds enhances its utility in creating complex fragrance formulations.
Beyond its role in perfumery, 1-(2-Methoxy-3,5-Dimethylphenyl)Ethanone has also found applications in materials science. Recent studies have highlighted its potential as a precursor for the synthesis of advanced polymers and coatings. Its reactivity under specific conditions allows for the formation of cross-linked structures with improved mechanical and thermal properties. This has led to its exploration in developing high-performance materials for aerospace and automotive industries.
In the pharmaceutical sector, 1-(2-Methoxy-3,5-Dimethylphenyl)Ethanone serves as an intermediate in drug synthesis. Its structural features make it an ideal candidate for modifying bioactive molecules to enhance their pharmacokinetic profiles. For example, researchers have utilized this compound as a building block for developing analogs of existing drugs with improved efficacy and reduced side effects.
The environmental impact of 1-(2-Methoxy-3,5-Dimethylphenyl)Ethanone has also been a subject of recent research. Studies have focused on understanding its biodegradation pathways and assessing its potential toxicity to aquatic life. These investigations are crucial for ensuring that the compound's use aligns with sustainability goals and regulatory standards.
In conclusion, 1-(2-Methoxy-3,5-Dimethylphenyl)Ethanone (CAS No. 147623-18-5) is a multifaceted compound with diverse applications across various industries. Its unique chemical structure and reactivity continue to drive innovative research and development efforts. As advancements in synthetic methodologies and application technologies progress, this compound is poised to play an even more significant role in shaping future products and technologies.
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