1-(Pyridin-2-yl)-1H-pyrazole-4-sulfonyl chloride

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Reagent Code: #222663
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CAS Number 1097223-12-5

science Other reagents with same CAS 1097223-12-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.67 g/mol
Formula C₈H₆N₃O₂SCl
badge Registry Numbers
MDL Number MFCD12192690
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its sulfonyl chloride group readily reacts with nucleophiles, enabling the formation of sulfonamides and sulfonate esters that are important in bioactive molecule design. Commonly employed in medicinal chemistry for constructing kinase inhibitors and other targeted therapies. Also utilized in the preparation of pyrazole-based compounds with potential antimicrobial and anti-inflammatory activities.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,340.00
inventory 1g
10-20 days ฿33,650.00

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1-(Pyridin-2-yl)-1H-pyrazole-4-sulfonyl chloride
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its sulfonyl chloride group readily reacts with nucleophiles, enabling the formation of sulfonamides and sulfonate esters that are important in bioactive molecule design. Commonly employed in medicinal chemistry for constructing kinase inhibitors and other targeted therapies. Also utilized in the preparation of pyrazole-based compounds with potential antimicrobia

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its sulfonyl chloride group readily reacts with nucleophiles, enabling the formation of sulfonamides and sulfonate esters that are important in bioactive molecule design. Commonly employed in medicinal chemistry for constructing kinase inhibitors and other targeted therapies. Also utilized in the preparation of pyrazole-based compounds with potential antimicrobial and anti-inflammatory activities.

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