N,N-Dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide
98%
Reagent
Code: #44441
CAS Number
486422-05-3
blur_circular Chemical Specifications
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Molecular Information
Weight
311.2000 g/mol
Formula
C₁₄H₂₂BNO₄S
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Registry Numbers
MDL Number
MFCD07368237
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Storage & Handling
Storage
room temperature
description Product Description
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drugs, bioactive compounds, and advanced materials. Additionally, it is utilized in research for designing and synthesizing novel compounds with potential therapeutic or industrial applications.
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