5-Isopropyl-2-methoxy-4-methylbenzene-1-sulfonyl chloride

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Reagent Code: #198564
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CAS Number 1216272-28-4

science Other reagents with same CAS 1216272-28-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.75 g/mol
Formula C₁₁H₁₅O₃SCl
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a sulfonating agent to introduce the sulfonyl chloride functional group into target molecules. Its reactivity allows for the formation of sulfonamides and sulfonate esters, which are key structural motifs in certain herbicides and fungicides. It is also employed in research settings for modifying bioactive molecules to enhance stability or alter solubility. Due to its sensitivity to moisture, it is handled under anhydrous conditions in controlled environments.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,900.00
inventory 1g
10-20 days ฿13,190.00
inventory 5g
10-20 days ฿46,100.00

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5-Isopropyl-2-methoxy-4-methylbenzene-1-sulfonyl chloride
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Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a sulfonating agent to introduce the sulfonyl chloride functional group into target molecules. Its reactivity allows for the formation of sulfonamides and sulfonate esters, which are key structural motifs in certain herbicides and fungicides. It is also employed in research settings for modifying bioactive molecules to enhance stability or alter solubility. Due to its sensitivity to moisture,

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a sulfonating agent to introduce the sulfonyl chloride functional group into target molecules. Its reactivity allows for the formation of sulfonamides and sulfonate esters, which are key structural motifs in certain herbicides and fungicides. It is also employed in research settings for modifying bioactive molecules to enhance stability or alter solubility. Due to its sensitivity to moisture, it is handled under anhydrous conditions in controlled environments.

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