5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-sulfonamide
97%
Reagent
Code: #119755
CAS Number
1083326-26-4
science Other reagents with same CAS 1083326-26-4
blur_circular Chemical Specifications
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Molecular Information
Weight
284.14 g/mol
Formula
C₁₁H₁₇BN₂O₄S
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Registry Numbers
MDL Number
MFCD13190590
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Physical Properties
Boiling Point
470.0±55.0°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, store under inert gas
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group acts as a key intermediate, enabling the formation of carbon-carbon bonds, which is essential in constructing complex molecules. It is often employed in the development of pharmaceuticals, where it aids in the synthesis of active pharmaceutical ingredients (APIs) and drug candidates. Additionally, its pyridine and sulfonamide moieties make it valuable in designing molecules with potential biological activity, such as enzyme inhibitors or receptor modulators. Researchers also use it in material science to create novel organic compounds with specific electronic or structural properties.
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