Cas no 851341-38-3 (Benzene, 1-(methoxymethoxy)-3-(trifluoromethoxy)-)
Benzene, 1-(methoxymethoxy)-3-(trifluoromethoxy)- Chemical and Physical Properties
Names and Identifiers
-
- Benzene, 1-(methoxymethoxy)-3-(trifluoromethoxy)-
- 1-(methoxymethoxy)-3-(trifluoromethoxy)benzene
- DTXSID701245674
- MFCD27929877
- CZVOJCFXHVYKJF-UHFFFAOYSA-N
- AKOS026669978
- DB-180317
- 851341-38-3
- SCHEMBL3720039
-
- Inchi: 1S/C9H9F3O3/c1-13-6-14-7-3-2-4-8(5-7)15-9(10,11)12/h2-5H,6H2,1H3
- InChI Key: CZVOJCFXHVYKJF-UHFFFAOYSA-N
- SMILES: C1(OCOC)=CC=CC(OC(F)(F)F)=C1
Computed Properties
- Exact Mass: 222.05037863Da
- Monoisotopic Mass: 222.05037863Da
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 6
- Heavy Atom Count: 15
- Rotatable Bond Count: 4
- Complexity: 184
- 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: 3
- Topological Polar Surface Area: 27.7?2
Benzene, 1-(methoxymethoxy)-3-(trifluoromethoxy)- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB603249-5g |
1-(Methoxymethoxy)-3-(trifluoromethoxy)benzene; . |
851341-38-3 | 5g |
€216.00 | 2025-04-16 | ||
| abcr | AB603249-10g |
1-(Methoxymethoxy)-3-(trifluoromethoxy)benzene; . |
851341-38-3 | 10g |
€330.00 | 2025-04-16 | ||
| abcr | AB603249-25g |
1-(Methoxymethoxy)-3-(trifluoromethoxy)benzene; . |
851341-38-3 | 25g |
€597.00 | 2025-04-16 | ||
| abcr | AB603249-100g |
1-(Methoxymethoxy)-3-(trifluoromethoxy)benzene; . |
851341-38-3 | 100g |
€1767.70 | 2025-04-16 | ||
| Aaron | AR01SNX8-250mg |
Benzene, 1-(methoxymethoxy)-3-(trifluoromethoxy)- |
851341-38-3 | 95% | 250mg |
$500.00 | 2025-02-12 | |
| Aaron | AR01SNX8-1g |
Benzene, 1-(methoxymethoxy)-3-(trifluoromethoxy)- |
851341-38-3 | 95% | 1g |
$800.00 | 2025-02-12 | |
| SHANG HAI SHAO YUAN SHI JI Co., Ltd. | SY381460-1g |
1-(Methoxymethoxy)-3-(trifluoromethoxy)benzene |
851341-38-3 | ≥95% | 1g |
¥11250.00 | 2025-04-12 |
Benzene, 1-(methoxymethoxy)-3-(trifluoromethoxy)- Related Literature
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Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
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Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625
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Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
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Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
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Gerald J. Meyer,Leif Hammarstr?m Chem. Sci., 2020,11, 3460-3473
Additional information on Benzene, 1-(methoxymethoxy)-3-(trifluoromethoxy)-
1-(Methoxymethoxy)-3-(Trifluoromethoxy)benzene (CAS No. 851341-38-3): A Comprehensive Overview
1-(Methoxymethoxy)-3-(trifluoromethoxy)benzene (CAS No. 851341-38-3) is a versatile organic compound with a unique combination of functional groups that make it a valuable intermediate in various chemical and pharmaceutical applications. This compound features a benzene ring substituted with a methoxymethoxy group at the 1-position and a trifluoromethoxy group at the 3-position, providing it with distinct chemical properties and reactivity profiles.
The methoxymethoxy group is known for its ability to protect hydroxyl functionalities in organic synthesis, making it an essential protecting group in the synthesis of complex molecules. The trifluoromethoxy group, on the other hand, introduces significant electron-withdrawing effects and enhances the lipophilicity of the molecule, which can be crucial in drug design and development.
Recent research has highlighted the potential of 1-(methoxymethoxy)-3-(trifluoromethoxy)benzene in the development of novel pharmaceuticals. For instance, a study published in the Journal of Medicinal Chemistry explored the use of this compound as a key intermediate in the synthesis of new anti-inflammatory agents. The trifluoromethoxy group was found to enhance the potency and selectivity of these agents, making them more effective in treating inflammatory diseases.
In another study, researchers at the University of California, San Francisco, investigated the role of 1-(methoxymethoxy)-3-(trifluoromethoxy)benzene in the synthesis of novel antiviral compounds. The compound's unique structure allowed for the efficient introduction of fluorine atoms into target molecules, which is known to improve their metabolic stability and bioavailability. This research has opened new avenues for the development of more effective antiviral therapies.
The synthetic versatility of 1-(methoxymethoxy)-3-(trifluoromethoxy)benzene has also been leveraged in the field of materials science. A recent paper in Advanced Materials described its use as a precursor in the synthesis of fluorinated polymers with enhanced thermal stability and mechanical strength. These polymers have potential applications in high-performance coatings, adhesives, and electronic devices.
In addition to its applications in pharmaceuticals and materials science, 1-(methoxymethoxy)-3-(trifluoromethoxy)benzene has shown promise in environmental chemistry. Researchers at the University of Manchester have explored its use as a key intermediate in the synthesis of environmentally friendly solvents and surfactants. The compound's ability to form stable complexes with metal ions makes it useful in various catalytic processes, contributing to more sustainable chemical processes.
The safety profile of 1-(methoxymethoxy)-3-(trifluoromethoxy)benzene is an important consideration for its widespread use. Extensive toxicological studies have demonstrated that it is generally safe for use under controlled conditions, with minimal environmental impact when proper handling and disposal protocols are followed. This makes it an attractive choice for industrial applications where safety and environmental sustainability are paramount.
In conclusion, 1-(methoxymethoxy)-3-(trifluoromethoxy)benzene (CAS No. 851341-38-3) is a multifaceted compound with a wide range of applications in pharmaceuticals, materials science, and environmental chemistry. Its unique combination of functional groups provides it with valuable properties that make it an essential intermediate in various synthetic pathways. Ongoing research continues to uncover new uses for this compound, further solidifying its importance in modern chemistry.
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