3-Bromoquinoline-5-sulfonyl chloride

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Reagent Code: #153287
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CAS Number 33768-83-1

science Other reagents with same CAS 33768-83-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.56 g/mol
Formula C₉H₅BrClNO₂S
badge Registry Numbers
MDL Number MFCD28671309
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a key intermediate in the synthesis of biologically active compounds, especially in pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. It is particularly useful in medicinal chemistry for developing kinase inhibitors and other targeted therapies due to the quinoline scaffold’s affinity for biological targets. Also employed in the preparation of fluorescent probes and dyes, leveraging the inherent fluorescence of the quinoline ring for sensing applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,440.00
inventory 250mg
10-20 days ฿32,140.00

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3-Bromoquinoline-5-sulfonyl chloride
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Used primarily as a key intermediate in the synthesis of biologically active compounds, especially in pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. It is particularly useful in medicinal chemistry for developing kinase inhibitors and other targeted therapies due to the quinoline scaffold’s affinity for biological targets. Also employed in the preparation of fluorescen

Used primarily as a key intermediate in the synthesis of biologically active compounds, especially in pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. It is particularly useful in medicinal chemistry for developing kinase inhibitors and other targeted therapies due to the quinoline scaffold’s affinity for biological targets. Also employed in the preparation of fluorescent probes and dyes, leveraging the inherent fluorescence of the quinoline ring for sensing applications.

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