5-[5-(Trifluoromethyl)isoxazol-3-yl]thiophene-2-sulfonyl chloride

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Reagent Code: #244813
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CAS Number 229956-98-3

science Other reagents with same CAS 229956-98-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 317.69 g/mol
Formula C₈H₃ClF₃NO₃S₂
badge Registry Numbers
MDL Number MFCD00831001
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines or alcohols to form sulfonamides or sulfonate esters, making it valuable in constructing sulfone-based derivatives. It is especially useful in drug discovery for developing kinase inhibitors and other therapeutic agents where the trifluoromethylisoxazole moiety enhances metabolic stability and binding affinity. Also employed in the preparation of functionalized thiophene derivatives for use in materials science, including organic semiconductors and electronic materials.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,140.00
inventory 5g
10-20 days ฿21,390.00
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5-[5-(Trifluoromethyl)isoxazol-3-yl]thiophene-2-sulfonyl chloride
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines or alcohols to form sulfonamides or sulfonate esters, making it valuable in constructing sulfone-based derivatives. It is especially useful in drug discovery for developing kinase inhibitors and other therapeutic agents where the trifluoromethylisoxazole moiety enhances metabolic stability and binding affinity. Also employe

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines or alcohols to form sulfonamides or sulfonate esters, making it valuable in constructing sulfone-based derivatives. It is especially useful in drug discovery for developing kinase inhibitors and other therapeutic agents where the trifluoromethylisoxazole moiety enhances metabolic stability and binding affinity. Also employed in the preparation of functionalized thiophene derivatives for use in materials science, including organic semiconductors and electronic materials.

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