4'-Trifluoromethyl-3,4-dimethoxybenzophenone

98%

Reagent Code: #244872
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CAS Number 116412-99-8

science Other reagents with same CAS 116412-99-8

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scatter_plot Molecular Information
Weight 310.27 g/mol
Formula C₁₆H₁₃F₃O₃
badge Registry Numbers
MDL Number MFCD16619235
inventory_2 Storage & Handling
Storage -20°C, Sealed

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and fine chemicals. Its structure supports the development of bioactive molecules, particularly in drug discovery where fluorinated compounds enhance metabolic stability and binding affinity. Commonly employed in the preparation of photoinitiators for UV-curable coatings and adhesives due to the benzophenone core, which facilitates efficient radical generation under UV light. The trifluoromethyl and methoxy groups improve solubility and electronic properties, making it suitable for use in advanced materials and organic electronic applications. Also utilized in the agrochemical industry for the development of herbicides and fungicides owing to its lipophilic nature and resistance to degradation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,930.00
inventory 1g
10-20 days ฿22,500.00

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4'-Trifluoromethyl-3,4-dimethoxybenzophenone
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Used primarily as an intermediate in the synthesis of pharmaceuticals and fine chemicals. Its structure supports the development of bioactive molecules, particularly in drug discovery where fluorinated compounds enhance metabolic stability and binding affinity. Commonly employed in the preparation of photoinitiators for UV-curable coatings and adhesives due to the benzophenone core, which facilitates efficient radical generation under UV light. The trifluoromethyl and methoxy groups improve solubility an

Used primarily as an intermediate in the synthesis of pharmaceuticals and fine chemicals. Its structure supports the development of bioactive molecules, particularly in drug discovery where fluorinated compounds enhance metabolic stability and binding affinity. Commonly employed in the preparation of photoinitiators for UV-curable coatings and adhesives due to the benzophenone core, which facilitates efficient radical generation under UV light. The trifluoromethyl and methoxy groups improve solubility and electronic properties, making it suitable for use in advanced materials and organic electronic applications. Also utilized in the agrochemical industry for the development of herbicides and fungicides owing to its lipophilic nature and resistance to degradation.

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