2-Thiophenesulfonamide

96%

Reagent Code: #239621
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Alias Thiophene-α-sulfonamide
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CAS Number 6339-87-3

science Other reagents with same CAS 6339-87-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.22 g/mol
Formula C₄H₅NO₂S₂
badge Registry Numbers
MDL Number MFCD00185853
thermostat Physical Properties
Melting Point 146-148°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs with antimicrobial, anti-inflammatory, and central nervous system modulating properties, including anti-epileptic and psychotropic agents. It also serves in the preparation of agrochemicals and dyes due to its reactive sulfonamide group and aromatic thiophene ring. Its structure allows for easy modification in organic synthesis, making it valuable in research and development of bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿280.00
inventory 5g
10-20 days ฿610.00
inventory 25g
10-20 days ฿2,300.00
inventory 100g
10-20 days ฿9,080.00
2-Thiophenesulfonamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs with antimicrobial, anti-inflammatory, and central nervous system modulating properties, including anti-epileptic and psychotropic agents. It also serves in the preparation of agrochemicals and dyes due to its reactive sulfonamide group and aromatic thiophene ring. Its structure allows for easy modification in organic synthesis, making it valuable in research and development of bioactiv

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs with antimicrobial, anti-inflammatory, and central nervous system modulating properties, including anti-epileptic and psychotropic agents. It also serves in the preparation of agrochemicals and dyes due to its reactive sulfonamide group and aromatic thiophene ring. Its structure allows for easy modification in organic synthesis, making it valuable in research and development of bioactive molecules.

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