1,3,5-Trimethyl-1H-pyrazole-4-sulfonyl chloride

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Reagent Code: #38883
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CAS Number 59340-27-1

science Other reagents with same CAS 59340-27-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.67 g/mol
Formula C₆H₉ClN₂O₂S
badge Registry Numbers
MDL Number MFCD02180944
thermostat Physical Properties
Boiling Point 312.4°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.45g/cm3
Storage 2-8°C, store under inert gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of sulfonamide derivatives, which are essential in pharmaceutical and agrochemical industries. It is employed in the development of bioactive compounds, including potential drug candidates, due to its reactivity in forming sulfonamide bonds. Additionally, it finds application in the synthesis of dyes, pigments, and other specialty chemicals, leveraging its sulfonyl chloride functional group for efficient chemical transformations. Its role in creating sulfonated polymers also contributes to materials science, particularly in producing polymers with specific functional properties.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿9,306.00
inventory 100mg
10-20 days ฿810.00
inventory 1g
10-20 days ฿2,646.00
inventory 250mg
10-20 days ฿1,206.00

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1,3,5-Trimethyl-1H-pyrazole-4-sulfonyl chloride
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Used as a key intermediate in organic synthesis, particularly in the preparation of sulfonamide derivatives, which are essential in pharmaceutical and agrochemical industries. It is employed in the development of bioactive compounds, including potential drug candidates, due to its reactivity in forming sulfonamide bonds. Additionally, it finds application in the synthesis of dyes, pigments, and other specialty chemicals, leveraging its sulfonyl chloride functional group for efficient chemical transformat

Used as a key intermediate in organic synthesis, particularly in the preparation of sulfonamide derivatives, which are essential in pharmaceutical and agrochemical industries. It is employed in the development of bioactive compounds, including potential drug candidates, due to its reactivity in forming sulfonamide bonds. Additionally, it finds application in the synthesis of dyes, pigments, and other specialty chemicals, leveraging its sulfonyl chloride functional group for efficient chemical transformations. Its role in creating sulfonated polymers also contributes to materials science, particularly in producing polymers with specific functional properties.

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