3-Cyanobenzene-1-sulfonyl fluoride

95%

Reagent Code: #156902
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CAS Number 402-27-7

science Other reagents with same CAS 402-27-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.18 g/mol
Formula C₇H₄FNO₂S
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MDL Number MFCD27950415
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key reagent in chemical biology and proteomics research, particularly in sulfur fluoride exchange (SuFEx) click chemistry. It acts as an electrophilic labeling agent that selectively reacts with nucleophilic amino acid residues such as lysine and tyrosine in proteins, enabling covalent modification for target identification and mapping protein interactions. Its high reactivity and stability make it valuable for developing activity-based protein profiling (ABPP) probes. Also employed in the synthesis of covalent inhibitors and functionalized biomolecules for drug discovery. Due to its ability to form stable sulfonate linkages, it is utilized in materials science for constructing robust polymer networks and functional surfaces.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,690.00
inventory 1g
10-20 days ฿4,580.00
inventory 5g
10-20 days ฿17,030.00

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3-Cyanobenzene-1-sulfonyl fluoride
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Used as a key reagent in chemical biology and proteomics research, particularly in sulfur fluoride exchange (SuFEx) click chemistry. It acts as an electrophilic labeling agent that selectively reacts with nucleophilic amino acid residues such as lysine and tyrosine in proteins, enabling covalent modification for target identification and mapping protein interactions. Its high reactivity and stability make it valuable for developing activity-based protein profiling (ABPP) probes. Also employed in the synt

Used as a key reagent in chemical biology and proteomics research, particularly in sulfur fluoride exchange (SuFEx) click chemistry. It acts as an electrophilic labeling agent that selectively reacts with nucleophilic amino acid residues such as lysine and tyrosine in proteins, enabling covalent modification for target identification and mapping protein interactions. Its high reactivity and stability make it valuable for developing activity-based protein profiling (ABPP) probes. Also employed in the synthesis of covalent inhibitors and functionalized biomolecules for drug discovery. Due to its ability to form stable sulfonate linkages, it is utilized in materials science for constructing robust polymer networks and functional surfaces.

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