3-(3,4-Dimethoxyphenyl)oxetane-3-sulfonyl fluoride

95%

Reagent Code: #131556
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CAS Number 2761834-03-9

science Other reagents with same CAS 2761834-03-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.28 g/mol
Formula C₁₁H₁₃FO₅S
thermostat Physical Properties
Boiling Point 407.1±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.40±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a highly selective reagent in chemical biology and medicinal chemistry for covalent protein modification. Its strained oxetane ring enhances reactivity, while the sulfonyl fluoride group enables stable bond formation with nucleophilic amino acid residues like lysine and tyrosine. This makes it valuable in developing targeted covalent inhibitors and probes for activity-based protein profiling. The compound’s stability under physiological conditions and selectivity allow for use in live-cell labeling and drug discovery applications. It is also employed in the synthesis of sulfonyl fluoride-containing molecules for use in SuFEx (Sulfur(VI) Fluoride Exchange) click chemistry, enabling rapid and reliable bioconjugation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,990.00
inventory 250mg
10-20 days ฿38,990.00

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3-(3,4-Dimethoxyphenyl)oxetane-3-sulfonyl fluoride
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Used as a highly selective reagent in chemical biology and medicinal chemistry for covalent protein modification. Its strained oxetane ring enhances reactivity, while the sulfonyl fluoride group enables stable bond formation with nucleophilic amino acid residues like lysine and tyrosine. This makes it valuable in developing targeted covalent inhibitors and probes for activity-based protein profiling. The compound’s stability under physiological conditions and selectivity allow for use in live-cell labeling
Used as a highly selective reagent in chemical biology and medicinal chemistry for covalent protein modification. Its strained oxetane ring enhances reactivity, while the sulfonyl fluoride group enables stable bond formation with nucleophilic amino acid residues like lysine and tyrosine. This makes it valuable in developing targeted covalent inhibitors and probes for activity-based protein profiling. The compound’s stability under physiological conditions and selectivity allow for use in live-cell labeling and drug discovery applications. It is also employed in the synthesis of sulfonyl fluoride-containing molecules for use in SuFEx (Sulfur(VI) Fluoride Exchange) click chemistry, enabling rapid and reliable bioconjugation.
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