5-Methylsulfonyl-2-(2,2,2-trifluoro-1-methylethoxy)benzoic acid methyl ester

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Reagent Code: #124415
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CAS Number 845617-19-8

science Other reagents with same CAS 845617-19-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 326.29 g/mol
Formula C₁₂H₁₃F₃O₅S
badge Registry Numbers
MDL Number MFCD25977306
thermostat Physical Properties
Boiling Point 422.8±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.343±0.06 g/cm3(Predicted)
Storage 2-8°C, dry, airtight

description Product Description

This compound is primarily utilized in the field of organic synthesis as an intermediate for the development of more complex chemical structures. Its unique functional groups make it valuable in the synthesis of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that require trifluoromethyl and sulfonyl groups for enhanced biological activity. Additionally, it is employed in research settings for the study of enzyme inhibition and receptor binding, where its structural features can be leveraged to design potent inhibitors or modulators. Its ester group also allows for further chemical modifications, making it a versatile building block in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿54,054.00

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5-Methylsulfonyl-2-(2,2,2-trifluoro-1-methylethoxy)benzoic acid methyl ester
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This compound is primarily utilized in the field of organic synthesis as an intermediate for the development of more complex chemical structures. Its unique functional groups make it valuable in the synthesis of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that require trifluoromethyl and sulfonyl groups for enhanced biological activity. Additionally, it is employed in research settings for the study of enzyme inhibition and receptor binding, where its structu

This compound is primarily utilized in the field of organic synthesis as an intermediate for the development of more complex chemical structures. Its unique functional groups make it valuable in the synthesis of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that require trifluoromethyl and sulfonyl groups for enhanced biological activity. Additionally, it is employed in research settings for the study of enzyme inhibition and receptor binding, where its structural features can be leveraged to design potent inhibitors or modulators. Its ester group also allows for further chemical modifications, making it a versatile building block in medicinal chemistry.

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