7-((Benzyloxy)methoxy)-4-(trifluoromethyl)-2H-chromen-2-one

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Reagent Code: #51328
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CAS Number 277309-33-8

science Other reagents with same CAS 277309-33-8

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Weight 350.2886 g/mol
Formula C₁₈H₁₃F₃O₄
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This compound is primarily utilized in organic synthesis and pharmaceutical research due to its unique structure, which includes a trifluoromethyl group and a chromen-2-one scaffold. It serves as a key intermediate in the development of biologically active molecules, particularly in the creation of compounds with potential anti-inflammatory, anticancer, or antimicrobial properties. The benzyloxy methoxy group enhances its reactivity, making it suitable for further chemical modifications. Additionally, its chromen-2-one core is often explored in the design of fluorescent probes or sensors for biochemical studies. Researchers also investigate its role in modulating enzyme activity or as a precursor for more complex heterocyclic compounds.

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inventory 25mg
10-20 days ฿8,784.00

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7-((Benzyloxy)methoxy)-4-(trifluoromethyl)-2H-chromen-2-one
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This compound is primarily utilized in organic synthesis and pharmaceutical research due to its unique structure, which includes a trifluoromethyl group and a chromen-2-one scaffold. It serves as a key intermediate in the development of biologically active molecules, particularly in the creation of compounds with potential anti-inflammatory, anticancer, or antimicrobial properties. The benzyloxy methoxy group enhances its reactivity, making it suitable for further chemical modifications. Additionally, it

This compound is primarily utilized in organic synthesis and pharmaceutical research due to its unique structure, which includes a trifluoromethyl group and a chromen-2-one scaffold. It serves as a key intermediate in the development of biologically active molecules, particularly in the creation of compounds with potential anti-inflammatory, anticancer, or antimicrobial properties. The benzyloxy methoxy group enhances its reactivity, making it suitable for further chemical modifications. Additionally, its chromen-2-one core is often explored in the design of fluorescent probes or sensors for biochemical studies. Researchers also investigate its role in modulating enzyme activity or as a precursor for more complex heterocyclic compounds.

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