1-(p-Toluenesulfonyl)pyrrole-2-boronic acid MIDA ester

Reagent Code: #242403
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CAS Number 1311484-50-0

science Other reagents with same CAS 1311484-50-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 376.19 g/mol
Formula C₁₆H₁₇BN₂O₆S
badge Registry Numbers
MDL Number MFCD15144862
thermostat Physical Properties
Melting Point 216-220°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions as a stable and selective boron reagent for constructing carbon-carbon bonds in complex molecule synthesis. Its MIDA ester group enhances stability and solubility, allowing for iterative coupling strategies in automated synthesis. Particularly valuable in pharmaceutical and agrochemical research for assembling heteroaromatic systems with high functional group tolerance. The p-toluenesulfonyl protection improves handling and shelf life compared to unprotected boronic acids.

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inventory 1g
10-20 days ฿4,550.00

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1-(p-Toluenesulfonyl)pyrrole-2-boronic acid MIDA ester
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Used in Suzuki-Miyaura cross-coupling reactions as a stable and selective boron reagent for constructing carbon-carbon bonds in complex molecule synthesis. Its MIDA ester group enhances stability and solubility, allowing for iterative coupling strategies in automated synthesis. Particularly valuable in pharmaceutical and agrochemical research for assembling heteroaromatic systems with high functional group tolerance. The p-toluenesulfonyl protection improves handling and shelf life compared to unprotecte

Used in Suzuki-Miyaura cross-coupling reactions as a stable and selective boron reagent for constructing carbon-carbon bonds in complex molecule synthesis. Its MIDA ester group enhances stability and solubility, allowing for iterative coupling strategies in automated synthesis. Particularly valuable in pharmaceutical and agrochemical research for assembling heteroaromatic systems with high functional group tolerance. The p-toluenesulfonyl protection improves handling and shelf life compared to unprotected boronic acids.

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