4-(pyridin-4-yloxy)benzene-1-sulfonyl chloride hydrochloride

≥95%

Reagent Code: #224928
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CAS Number 192330-49-7

science Other reagents with same CAS 192330-49-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 506.16 g/mol
Formula C₁₁H₉Cl₂NO₃S
badge Registry Numbers
MDL Number MFCD01631897
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceutical compounds. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide or sulfonate ester linkages. Commonly employed in the preparation of kinase inhibitors and other biologically active molecules. The pyridine moiety enhances binding affinity in drug candidates, particularly in medicinal chemistry targeting inflammatory and oncological pathways. Stable enough for use in solid-phase synthesis and compatible with various protection strategies in multi-step reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,520.00
inventory 250mg
10-20 days ฿5,000.00

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4-(pyridin-4-yloxy)benzene-1-sulfonyl chloride hydrochloride
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Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceutical compounds. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide or sulfonate ester linkages. Commonly employed in the preparation of kinase inhibitors and other biologically active molecules. The pyridine moiety enhances binding affinity in drug candidates, particularly in medicinal chemistry targeting inflammatory and oncological pathways

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceutical compounds. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide or sulfonate ester linkages. Commonly employed in the preparation of kinase inhibitors and other biologically active molecules. The pyridine moiety enhances binding affinity in drug candidates, particularly in medicinal chemistry targeting inflammatory and oncological pathways. Stable enough for use in solid-phase synthesis and compatible with various protection strategies in multi-step reactions.

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