1-Methyl-1H-Pyrazole-3-Sulfonyl Chloride

98%

Reagent Code: #207690
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CAS Number 89501-90-6

science Other reagents with same CAS 89501-90-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.61 g/mol
Formula C₄H₅ClN₂O₂S
badge Registry Numbers
MDL Number MFCD08690273
thermostat Physical Properties
Boiling Point 295.672ºC
inventory_2 Storage & Handling
Density 1.605g/cm3
Storage Room temperature, dry

description Product Description

Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals. Its sulfonyl chloride group readily reacts with nucleophiles, making it valuable for constructing sulfonamide linkages commonly found in bioactive molecules. It plays a significant role in the development of herbicides and fungicides due to the pyrazole ring’s ability to enhance target specificity and metabolic stability. Also employed in medicinal chemistry for building blocks in kinase inhibitors and anti-inflammatory agents. Its methyl group aids in modulating electronic properties and solubility in organic solvents, facilitating efficient reaction conditions in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,210.00
inventory 1g
10-20 days ฿3,840.00

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1-Methyl-1H-Pyrazole-3-Sulfonyl Chloride
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Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals. Its sulfonyl chloride group readily reacts with nucleophiles, making it valuable for constructing sulfonamide linkages commonly found in bioactive molecules. It plays a significant role in the development of herbicides and fungicides due to the pyrazole ring’s ability to enhance target specificity and metabolic stability. Also employed in medicinal chemistry for building blocks in kinase inhibitors and anti-inflam

Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals. Its sulfonyl chloride group readily reacts with nucleophiles, making it valuable for constructing sulfonamide linkages commonly found in bioactive molecules. It plays a significant role in the development of herbicides and fungicides due to the pyrazole ring’s ability to enhance target specificity and metabolic stability. Also employed in medicinal chemistry for building blocks in kinase inhibitors and anti-inflammatory agents. Its methyl group aids in modulating electronic properties and solubility in organic solvents, facilitating efficient reaction conditions in multi-step syntheses.

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