3-Methylthiophene-2-sulfonyl chloride

95%

Reagent Code: #214264
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CAS Number 61714-76-9

science Other reagents with same CAS 61714-76-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.68 g/mol
Formula C₅H₅ClO₂S₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where sulfonyl chloride groups act as coupling agents. Its reactivity allows for the introduction of sulfonyl functionalities into larger molecules, enabling the construction of sulfonamide-based drugs, which are common in antimicrobial, antidiabetic, and anti-inflammatory agents. Also employed in agrochemical synthesis for creating herbicides and pesticides due to its ability to modify aromatic systems with sulfur-containing groups. Its derivatives are valuable in materials science for designing organic semiconductors and conductive polymers, where the thiophene ring enhances electron delocalization. Commonly used in research laboratories for functionalizing complex molecules in medicinal chemistry campaigns.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10g
10-20 days ฿30,040.00
3-Methylthiophene-2-sulfonyl chloride
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Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where sulfonyl chloride groups act as coupling agents. Its reactivity allows for the introduction of sulfonyl functionalities into larger molecules, enabling the construction of sulfonamide-based drugs, which are common in antimicrobial, antidiabetic, and anti-inflammatory agents. Also employed in agrochemical synthesis for creating herbicides and pesticide

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where sulfonyl chloride groups act as coupling agents. Its reactivity allows for the introduction of sulfonyl functionalities into larger molecules, enabling the construction of sulfonamide-based drugs, which are common in antimicrobial, antidiabetic, and anti-inflammatory agents. Also employed in agrochemical synthesis for creating herbicides and pesticides due to its ability to modify aromatic systems with sulfur-containing groups. Its derivatives are valuable in materials science for designing organic semiconductors and conductive polymers, where the thiophene ring enhances electron delocalization. Commonly used in research laboratories for functionalizing complex molecules in medicinal chemistry campaigns.

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