5-Bromothiophene-2-sulfonyl fluoride

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Reagent Code: #120245
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CAS Number 108158-00-5

science Other reagents with same CAS 108158-00-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.08 g/mol
Formula C₄H₂BrFO₂S₂
badge Registry Numbers
MDL Number MFCD21894405
inventory_2 Storage & Handling
Density 1.8803 at 25 °C
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily used in organic synthesis as a versatile building block for the development of more complex molecules. It is particularly valuable in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of pharmaceutical compounds. Its sulfonyl fluoride group makes it a useful reagent for click chemistry reactions, enabling the formation of stable covalent bonds with target molecules. Additionally, it is employed in material science for the modification of polymers and surfaces, enhancing their properties for specific applications. Its bromine substituent allows for further functionalization, making it a flexible component in the design of advanced materials and bioactive compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿19,440.00
inventory 250mg
10-20 days ฿7,200.00
inventory 100mg
10-20 days ฿4,239.00

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5-Bromothiophene-2-sulfonyl fluoride
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This chemical is primarily used in organic synthesis as a versatile building block for the development of more complex molecules. It is particularly valuable in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of pharmaceutical compounds. Its sulfonyl fluoride group makes it a useful reagent for click chemistry reactions, enabling the formation of stable covalent bonds with target molecules. Additionally, it is employed in material science for the modification of p

This chemical is primarily used in organic synthesis as a versatile building block for the development of more complex molecules. It is particularly valuable in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of pharmaceutical compounds. Its sulfonyl fluoride group makes it a useful reagent for click chemistry reactions, enabling the formation of stable covalent bonds with target molecules. Additionally, it is employed in material science for the modification of polymers and surfaces, enhancing their properties for specific applications. Its bromine substituent allows for further functionalization, making it a flexible component in the design of advanced materials and bioactive compounds.

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