2-Propyne-1-sulfonyl Chloride

≥95%

Reagent Code: #228328
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CAS Number 32623-88-4

science Other reagents with same CAS 32623-88-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.57 g/mol
Formula C₃H₃ClO₂S
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry, Lightproof, Inert Gas

description Product Description

Used primarily as a reagent in organic synthesis, particularly in the preparation of sulfonate esters and sulfonamides. It acts as a sulfonylating agent, introducing the propynylsulfonyl group to nucleophiles such as alcohols and amines. This functionality is valuable in medicinal chemistry for modifying bioactive molecules, enhancing their stability or altering their reactivity. It is also employed in the development of specialty polymers and agrochemicals where unique sulfonyl linkages are required. Due to the presence of the alkyne group, it can participate in click chemistry reactions, enabling efficient conjugation in complex molecule assembly, such as in drug discovery and bioconjugation applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,120.00
inventory 1g
10-20 days ฿38,830.00
2-Propyne-1-sulfonyl Chloride
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Used primarily as a reagent in organic synthesis, particularly in the preparation of sulfonate esters and sulfonamides. It acts as a sulfonylating agent, introducing the propynylsulfonyl group to nucleophiles such as alcohols and amines. This functionality is valuable in medicinal chemistry for modifying bioactive molecules, enhancing their stability or altering their reactivity. It is also employed in the development of specialty polymers and agrochemicals where unique sulfonyl linkages are required. Du

Used primarily as a reagent in organic synthesis, particularly in the preparation of sulfonate esters and sulfonamides. It acts as a sulfonylating agent, introducing the propynylsulfonyl group to nucleophiles such as alcohols and amines. This functionality is valuable in medicinal chemistry for modifying bioactive molecules, enhancing their stability or altering their reactivity. It is also employed in the development of specialty polymers and agrochemicals where unique sulfonyl linkages are required. Due to the presence of the alkyne group, it can participate in click chemistry reactions, enabling efficient conjugation in complex molecule assembly, such as in drug discovery and bioconjugation applications.

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