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Atomfair Benzene, 1-methoxy-4-phenoxy- C13H12O2
Description 1-Methoxy-4-phenoxybenzene (CAS No. 1655-69-2) is a high-purity aromatic ether compound with the molecular formula C13H12O2. This specialty chemical is characterized by its clear to pale-yellow appearance and is widely utilized in organic synthesis and material science research. With a molecular weight of 200.23 g/mol, it exhibits excellent solubility in common organic solvents such as ethanol, acetone, and dichloromethane. Our product is rigorously tested for purity (??98% by GC) and is supplied in sealed glass vials or bulk packaging to ensure stability and longevity. Ideal for researchers investigating ether-based polymers, liquid crystals, or photochemical applications, this compound is handled under…
Description
Description
1-Methoxy-4-phenoxybenzene (CAS No. 1655-69-2) is a high-purity aromatic ether compound with the molecular formula C13H12O2. This specialty chemical is characterized by its clear to pale-yellow appearance and is widely utilized in organic synthesis and material science research. With a molecular weight of 200.23 g/mol, it exhibits excellent solubility in common organic solvents such as ethanol, acetone, and dichloromethane. Our product is rigorously tested for purity (??98% by GC) and is supplied in sealed glass vials or bulk packaging to ensure stability and longevity. Ideal for researchers investigating ether-based polymers, liquid crystals, or photochemical applications, this compound is handled under strict quality control to meet the demands of advanced scientific studies.
- CAS No: 1655-69-2
- Molecular Formula: C13H12O2
- Molecular Weight: 200.23
- Exact Mass: 200.083729621
- Monoisotopic Mass: 200.083729621
- IUPAC Name: 1-methoxy-4-phenoxybenzene
- SMILES: COC1=CC=C(C=C1)OC2=CC=CC=C2
- Synonyms: 1-Methoxy-4-phenoxybenzene, Benzene, 1-methoxy-4-phenoxy-, AI3-32896, DTXSID2061852, NSC 18747
Application
1-Methoxy-4-phenoxybenzene serves as a versatile intermediate in the synthesis of advanced materials, including liquid crystals and photoactive polymers. Researchers employ it in the development of organic semiconductors due to its electron-donating methoxy and phenoxy groups. It is also explored in supramolecular chemistry for constructing host-guest systems. Additionally, this compound finds use in fragrance and dye industries as a precursor for specialized derivatives.
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