3-(4-Methoxyphenyl)oxetane-3-sulfonyl fluoride

95%

Reagent Code: #130080
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CAS Number 2761830-88-8

science Other reagents with same CAS 2761830-88-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.26 g/mol
Formula C₁₀H₁₁FO₄S
thermostat Physical Properties
Boiling Point 380.0±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.41±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a highly reactive building block in medicinal chemistry, particularly in the development of covalent inhibitors. Its strained oxetane ring enhances binding affinity and metabolic stability in drug candidates. The sulfonyl fluoride group enables selective covalent modification of proteins, making it valuable in chemical biology for target identification and labeling. It is also employed in sulfur fluoride exchange (SuFEx) click chemistry, a robust method for assembling molecules under mild conditions, useful in drug discovery and bioconjugation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,390.00
inventory 250mg
10-20 days ฿17,640.00

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3-(4-Methoxyphenyl)oxetane-3-sulfonyl fluoride
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Used as a highly reactive building block in medicinal chemistry, particularly in the development of covalent inhibitors. Its strained oxetane ring enhances binding affinity and metabolic stability in drug candidates. The sulfonyl fluoride group enables selective covalent modification of proteins, making it valuable in chemical biology for target identification and labeling. It is also employed in sulfur fluoride exchange (SuFEx) click chemistry, a robust method for assembling molecules under mild conditions
Used as a highly reactive building block in medicinal chemistry, particularly in the development of covalent inhibitors. Its strained oxetane ring enhances binding affinity and metabolic stability in drug candidates. The sulfonyl fluoride group enables selective covalent modification of proteins, making it valuable in chemical biology for target identification and labeling. It is also employed in sulfur fluoride exchange (SuFEx) click chemistry, a robust method for assembling molecules under mild conditions, useful in drug discovery and bioconjugation.
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