Trifluoromethyl 4-methylbenzenesulfonate

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Reagent Code: #84212
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CAS Number 175676-42-3

science Other reagents with same CAS 175676-42-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.20 g/mol
Formula C₈H₇F₃O₃S
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MDL Number MFCD31695793
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Trifluoromethyl 4-methylbenzenesulfonate is widely used as a reagent in organic synthesis, particularly for introducing the trifluoromethyl group into various organic compounds. This functional group is highly valued in pharmaceuticals and agrochemicals due to its ability to enhance metabolic stability, bioavailability, and lipophilicity of the molecules. The compound is often employed in nucleophilic substitution reactions, where it acts as an effective trifluoromethylating agent, enabling the synthesis of complex molecules with trifluoromethyl groups. Additionally, it is utilized in the development of advanced materials, such as polymers and liquid crystals, where the trifluoromethyl group can impart unique electronic and physical properties. Its application in medicinal chemistry is particularly notable, as it aids in the creation of drug candidates with improved efficacy and reduced side effects.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,524.00
inventory 100mg
10-20 days ฿2,214.00
inventory 250mg
10-20 days ฿3,105.00
inventory 5g
10-20 days ฿27,828.00

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Trifluoromethyl 4-methylbenzenesulfonate
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Trifluoromethyl 4-methylbenzenesulfonate is widely used as a reagent in organic synthesis, particularly for introducing the trifluoromethyl group into various organic compounds. This functional group is highly valued in pharmaceuticals and agrochemicals due to its ability to enhance metabolic stability, bioavailability, and lipophilicity of the molecules. The compound is often employed in nucleophilic substitution reactions, where it acts as an effective trifluoromethylating agent, enabling the synthesis

Trifluoromethyl 4-methylbenzenesulfonate is widely used as a reagent in organic synthesis, particularly for introducing the trifluoromethyl group into various organic compounds. This functional group is highly valued in pharmaceuticals and agrochemicals due to its ability to enhance metabolic stability, bioavailability, and lipophilicity of the molecules. The compound is often employed in nucleophilic substitution reactions, where it acts as an effective trifluoromethylating agent, enabling the synthesis of complex molecules with trifluoromethyl groups. Additionally, it is utilized in the development of advanced materials, such as polymers and liquid crystals, where the trifluoromethyl group can impart unique electronic and physical properties. Its application in medicinal chemistry is particularly notable, as it aids in the creation of drug candidates with improved efficacy and reduced side effects.

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