4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxamide
97%
Reagent
Code: #243619
CAS Number
957345-71-0
blur_circular Chemical Specifications
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Storage & Handling
Storage
2-8°C, light-proof, inert gas
description Product Description
Used in organic synthesis as a key building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronate ester group facilitates mild and selective coupling with aryl or heteroaryl halides, making it valuable in the preparation of complex thiophene-based structures. The carboxamide functionality adds polarity and hydrogen-bonding capability, which can enhance solubility and influence the biological activity of target molecules. Commonly employed in the synthesis of conjugated materials for optoelectronics and in medicinal chemistry for designing kinase inhibitors and other bioactive compounds.
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