Imidazo[1,2-a]pyridine-3-sulfonyl chloride

95%

Reagent Code: #198651
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CAS Number 499770-78-4

science Other reagents with same CAS 499770-78-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.64 g/mol
Formula C₇H₅ClN₂O₂S
badge Registry Numbers
MDL Number MFCD03407340
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with nucleophiles like amines and alcohols, enabling the formation of sulfonamides and sulfonate esters—common motifs in drug design. It plays a significant role in developing kinase inhibitors and antimicrobial agents due to the imidazopyridine core’s favorable binding properties with biological targets. Also employed in combinatorial chemistry for generating compound libraries in medicinal research.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10g
10-20 days ฿333,390.00
Imidazo[1,2-a]pyridine-3-sulfonyl chloride
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with nucleophiles like amines and alcohols, enabling the formation of sulfonamides and sulfonate esters—common motifs in drug design. It plays a significant role in developing kinase inhibitors and antimicrobial agents due to the imidazopyridine core’s favorable binding properties with biological targets. Also employed in combinatorial

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with nucleophiles like amines and alcohols, enabling the formation of sulfonamides and sulfonate esters—common motifs in drug design. It plays a significant role in developing kinase inhibitors and antimicrobial agents due to the imidazopyridine core’s favorable binding properties with biological targets. Also employed in combinatorial chemistry for generating compound libraries in medicinal research.

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