4H-1,2,4-Triazole-3-sulfonyl chloride

97%

Reagent Code: #196680
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Alias 1H-1,2,4-triazole-5-sulfonyl chloride
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CAS Number 6461-29-6

science Other reagents with same CAS 6461-29-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.57 g/mol
Formula C₂H₂ClN₃O₂S
badge Registry Numbers
MDL Number MFCD09972083
thermostat Physical Properties
Melting Point 122-124 °C
Boiling Point 425.191 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Widely used in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a key intermediate in the preparation of sulfonyl derivatives. Its reactivity allows for the introduction of the triazole ring system into larger molecules, enhancing biological activity in crop protection agents and medicinal compounds. It is particularly valuable in creating herbicides and fungicides due to the stability and bioavailability imparted by the triazole moiety. Additionally, it participates in the development of coordination compounds and functional materials where sulfonyl chloride groups enable further chemical modifications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,760.00
inventory 250mg
10-20 days ฿6,360.00
inventory 1g
10-20 days ฿18,890.00

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4H-1,2,4-Triazole-3-sulfonyl chloride
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Widely used in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a key intermediate in the preparation of sulfonyl derivatives. Its reactivity allows for the introduction of the triazole ring system into larger molecules, enhancing biological activity in crop protection agents and medicinal compounds. It is particularly valuable in creating herbicides and fungicides due to the stability and bioavailability imparted by the triazole moiety. Additionally, it participates in the dev

Widely used in the synthesis of agrochemicals and pharmaceuticals, this compound serves as a key intermediate in the preparation of sulfonyl derivatives. Its reactivity allows for the introduction of the triazole ring system into larger molecules, enhancing biological activity in crop protection agents and medicinal compounds. It is particularly valuable in creating herbicides and fungicides due to the stability and bioavailability imparted by the triazole moiety. Additionally, it participates in the development of coordination compounds and functional materials where sulfonyl chloride groups enable further chemical modifications.

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