4-(Pent-1-Yl)Benzenesulphonyl Chloride

99%

Reagent Code: #227871
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CAS Number 73948-18-2

science Other reagents with same CAS 73948-18-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.76 g/mol
Formula C₁₁H₁₅ClO₂S
inventory_2 Storage & Handling
Density 1.183±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide derivatives which have applications in pharmaceuticals and agrochemicals. Its reactivity allows for the introduction of sulfonyl chloride functional groups into complex molecules, facilitating the development of bioactive compounds. Commonly employed in the synthesis of herbicides and fungicides due to the stability and electron-withdrawing nature of the sulfonyl chloride moiety. Also utilized in research settings for modifying aromatic systems in drug discovery programs.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,460.00
250mg
10-20 days ฿1,830.00
4-(Pent-1-Yl)Benzenesulphonyl Chloride
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Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide derivatives which have applications in pharmaceuticals and agrochemicals. Its reactivity allows for the introduction of sulfonyl chloride functional groups into complex molecules, facilitating the development of bioactive compounds. Commonly employed in the synthesis of herbicides and fungicides due to the stability and electron-withdrawing nature of the sulfonyl chloride moiety. Also utilized in research setting

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide derivatives which have applications in pharmaceuticals and agrochemicals. Its reactivity allows for the introduction of sulfonyl chloride functional groups into complex molecules, facilitating the development of bioactive compounds. Commonly employed in the synthesis of herbicides and fungicides due to the stability and electron-withdrawing nature of the sulfonyl chloride moiety. Also utilized in research settings for modifying aromatic systems in drug discovery programs.

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