3-(Bromomethyl)benzene-1-sulfonyl fluoride

95%

Reagent Code: #153539
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CAS Number 79686-36-5

science Other reagents with same CAS 79686-36-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.09 g/mol
Formula C₇H₆BrFO₂S
badge Registry Numbers
MDL Number MFCD31445396
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a highly reactive electrophilic reagent in organic synthesis, particularly in the development of covalent inhibitors for biological targets. Its sulfonyl fluoride group reacts selectively with nucleophilic amino acid residues such as serine, threonine, and lysine in enzymes, making it valuable in chemical biology for activity-based protein profiling (ABPP). The bromomethyl group allows for further functionalization via nucleophilic substitution, enabling conjugation to tags, probes, or solid supports. It is also employed in the synthesis of sulfonyl fluoride-containing compounds for use in medicinal chemistry and agrochemical research due to their stability and unique reactivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿12,380.00
250mg
10-20 days ฿16,770.00
1g
10-20 days ฿54,110.00
3-(Bromomethyl)benzene-1-sulfonyl fluoride
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Used as a highly reactive electrophilic reagent in organic synthesis, particularly in the development of covalent inhibitors for biological targets. Its sulfonyl fluoride group reacts selectively with nucleophilic amino acid residues such as serine, threonine, and lysine in enzymes, making it valuable in chemical biology for activity-based protein profiling (ABPP). The bromomethyl group allows for further functionalization via nucleophilic substitution, enabling conjugation to tags, probes, or solid supp

Used as a highly reactive electrophilic reagent in organic synthesis, particularly in the development of covalent inhibitors for biological targets. Its sulfonyl fluoride group reacts selectively with nucleophilic amino acid residues such as serine, threonine, and lysine in enzymes, making it valuable in chemical biology for activity-based protein profiling (ABPP). The bromomethyl group allows for further functionalization via nucleophilic substitution, enabling conjugation to tags, probes, or solid supports. It is also employed in the synthesis of sulfonyl fluoride-containing compounds for use in medicinal chemistry and agrochemical research due to their stability and unique reactivity.

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