4-(Phenylsulfonyl)thiophene-2-sulfonyl chloride

97%

Reagent Code: #222691
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CAS Number 160233-28-3

science Other reagents with same CAS 160233-28-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.81 g/mol
Formula C₁₀H₇ClO₄S₃
badge Registry Numbers
MDL Number MFCD00052138
thermostat Physical Properties
Melting Point 101 °C
Boiling Point 519.7±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.582±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its dual sulfonyl functionality allows for sequential derivatization, enabling the construction of complex sulfone-based structures. Commonly employed in the development of sulfonamide drugs due to its ability to react selectively with amines. Also utilized in materials science for designing electron-accepting units in organic semiconductors. Its reactivity makes it valuable in cross-coupling reactions and heterocyclic chemistry for building sulfur-containing scaffolds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,120.00
inventory 250mg
10-20 days ฿18,240.00
inventory 1g
10-20 days ฿63,800.00
4-(Phenylsulfonyl)thiophene-2-sulfonyl chloride
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its dual sulfonyl functionality allows for sequential derivatization, enabling the construction of complex sulfone-based structures. Commonly employed in the development of sulfonamide drugs due to its ability to react selectively with amines. Also utilized in materials science for designing electron-accepting units in organic semiconductors. Its reactivity makes it valuable in cr
Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its dual sulfonyl functionality allows for sequential derivatization, enabling the construction of complex sulfone-based structures. Commonly employed in the development of sulfonamide drugs due to its ability to react selectively with amines. Also utilized in materials science for designing electron-accepting units in organic semiconductors. Its reactivity makes it valuable in cross-coupling reactions and heterocyclic chemistry for building sulfur-containing scaffolds.
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