3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

95%

Reagent Code: #91216
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CAS Number 486422-08-6

science Other reagents with same CAS 486422-08-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.15 g/mol
Formula C₁₂H₁₈BNO₄S
badge Registry Numbers
MDL Number MFCD07781217
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. The boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of various bioactive compounds and drug candidates. Additionally, it is utilized in materials science for creating advanced polymers and organic electronic materials. Its sulfonamide moiety also makes it valuable in designing molecules with potential biological activity, such as enzyme inhibitors or antimicrobial agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,907.00
inventory 1g
10-20 days ฿5,850.00

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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide
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This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. The boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of various bioactive compounds and drug candidates. Additionally, it is utilized in materials science for creating advanced polymers and organic electronic materials. Its sulfonami

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. The boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of various bioactive compounds and drug candidates. Additionally, it is utilized in materials science for creating advanced polymers and organic electronic materials. Its sulfonamide moiety also makes it valuable in designing molecules with potential biological activity, such as enzyme inhibitors or antimicrobial agents.

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