Cas no 851341-38-3 (Benzene, 1-(methoxymethoxy)-3-(trifluoromethoxy)-)

Benzene, 1-(methoxymethoxy)-3-(trifluoromethoxy)- is a specialized aromatic compound featuring both methoxymethoxy and trifluoromethoxy functional groups. Its unique structure contributes to enhanced reactivity and stability, making it valuable in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals. The trifluoromethoxy group imparts electron-withdrawing properties, while the methoxymethoxy group offers versatility in further functionalization. This compound is particularly useful as an intermediate in multi-step synthesis, enabling precise modifications to aromatic frameworks. Its well-defined reactivity profile ensures consistent performance in coupling reactions and other transformations, supporting the efficient production of complex molecules. Proper handling under controlled conditions is recommended due to its potential sensitivity.
Benzene, 1-(methoxymethoxy)-3-(trifluoromethoxy)- structure
851341-38-3 structure
Product Name:Benzene, 1-(methoxymethoxy)-3-(trifluoromethoxy)-
CAS No:851341-38-3
MF:C9H9F3O3
MW:222.161173582077
CID:4231232
PubChem ID:12179650
Update Time:2025-10-31

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 >>

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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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