Ethyl 3-methyl-4-(trifluoromethyl)benzoate

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Reagent Code: #184842
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CAS Number 1214387-66-2

science Other reagents with same CAS 1214387-66-2

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scatter_plot Molecular Information
Weight 232.202 g/mol
Formula C₁₁H₁₁F₃O₂
badge Registry Numbers
MDL Number MFCD14698275
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its ester functionality allows for further chemical modifications, making it valuable in building complex organic molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the presence of the trifluoromethyl group, which can influence lipophilicity and binding affinity. Also utilized in the preparation of specialty chemicals where fluorine substitution is desired for improved performance.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,670.00
inventory 250mg
10-20 days ฿3,950.00
inventory 1g
10-20 days ฿12,090.00

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Ethyl 3-methyl-4-(trifluoromethyl)benzoate
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its ester functionality allows for further chemical modifications, making it valuable in building complex organic molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the presence of the trifluoromethyl group, which can influence lipophilicity and binding affinity. Al

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its ester functionality allows for further chemical modifications, making it valuable in building complex organic molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the presence of the trifluoromethyl group, which can influence lipophilicity and binding affinity. Also utilized in the preparation of specialty chemicals where fluorine substitution is desired for improved performance.

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