5-Methyl-3-pyridinesulfonyl chloride

97%

Reagent Code: #210072
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CAS Number 166337-57-1

science Other reagents with same CAS 166337-57-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.64 g/mol
Formula C₆H₆ClNO₂S
badge Registry Numbers
MDL Number MFCD13188992
inventory_2 Storage & Handling
Storage 2-8℃, inert gas storage

description Product Description

Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its sulfonyl chloride functional group allows for easy attachment to other molecules, making it valuable in constructing sulfonamide-based compounds. It is also employed in the preparation of pyridine derivatives with biological activity, including those explored for use in crop protection products. The compound's reactivity supports its role in coupling reactions during the manufacturing of complex organic molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,920.00
inventory 250mg
10-20 days ฿16,630.00
inventory 1g
10-20 days ฿57,750.00
5-Methyl-3-pyridinesulfonyl chloride
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Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its sulfonyl chloride functional group allows for easy attachment to other molecules, making it valuable in constructing sulfonamide-based compounds. It is also employed in the preparation of pyridine derivatives with biological activity, including those explored for use in crop protection products. The compound's reactivity supports its ro

Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its sulfonyl chloride functional group allows for easy attachment to other molecules, making it valuable in constructing sulfonamide-based compounds. It is also employed in the preparation of pyridine derivatives with biological activity, including those explored for use in crop protection products. The compound's reactivity supports its role in coupling reactions during the manufacturing of complex organic molecules.

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