4-(Pyridin-2-Yloxy)Benzene-1-Sulfonyl Chloride

95%

Reagent Code: #227033
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CAS Number 192329-94-5

science Other reagents with same CAS 192329-94-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.70 g/mol
Formula C₁₁H₈ClNO₃S
badge Registry Numbers
MDL Number MFCD09755965
thermostat Physical Properties
Melting Point 158 °C
Boiling Point 392.1±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.420±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert gas storage

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. It is also employed in medicinal chemistry for modifying bioactive molecules to enhance their stability and binding properties. Commonly utilized in research settings for the preparation of kinase inhibitors and other biologically active compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,280.00
inventory 250mg
10-20 days ฿9,600.00
inventory 1g
10-20 days ฿28,800.00

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4-(Pyridin-2-Yloxy)Benzene-1-Sulfonyl Chloride
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. It is also employed in medicinal chemistry for modifying bioactive molecules to enhance their stability and binding properties. Commonly utilized in research settings for the preparation of kinase inhibitors and oth

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. It is also employed in medicinal chemistry for modifying bioactive molecules to enhance their stability and binding properties. Commonly utilized in research settings for the preparation of kinase inhibitors and other biologically active compounds.

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