6-MORPHOLIN-4-YL-PYRIDINE-3-SULFONYL CHLORIDE

97%

Reagent Code: #214468
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CAS Number 337508-68-6

science Other reagents with same CAS 337508-68-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.71 g/mol
Formula C₉H₁₁ClN₂O₃S
badge Registry Numbers
MDL Number MFCD02681929
thermostat Physical Properties
Melting Point 118 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It participates in sulfa coupling reactions to form sulfonamides, which are key structural motifs in various bioactive molecules and drug candidates. Its reactivity with amines makes it valuable for introducing the pyridine-morpholine sulfonamide group into larger compounds, often explored in kinase inhibitor development and medicinal chemistry research. Due to the presence of the morpholine and pyridine rings, it contributes to improved solubility and binding affinity in target molecules. Commonly handled under anhydrous conditions due to the sensitivity of the sulfonyl chloride group to moisture.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿66,900.00
6-MORPHOLIN-4-YL-PYRIDINE-3-SULFONYL CHLORIDE
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It participates in sulfa coupling reactions to form sulfonamides, which are key structural motifs in various bioactive molecules and drug candidates. Its reactivity with amines makes it valuable for introducing the pyridine-morpholine sulfonamide group into larger compounds, often explored in kinase inhibitor development and medicinal chemistry research. Due to the presence of the morpholine and pyridine ri

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It participates in sulfa coupling reactions to form sulfonamides, which are key structural motifs in various bioactive molecules and drug candidates. Its reactivity with amines makes it valuable for introducing the pyridine-morpholine sulfonamide group into larger compounds, often explored in kinase inhibitor development and medicinal chemistry research. Due to the presence of the morpholine and pyridine rings, it contributes to improved solubility and binding affinity in target molecules. Commonly handled under anhydrous conditions due to the sensitivity of the sulfonyl chloride group to moisture.

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