4,4,5,5-tetramethyl-2-(5-phenylthiophen-2-yl)-1,3,2-dioxaborolane
98%
Reagent
Code: #241557
CAS Number
459409-74-6
blur_circular Chemical Specifications
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Molecular Information
Weight
286.197 g/mol
Formula
C₁₆H₁₉BO₂S
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Registry Numbers
MDL Number
MFCD08063141
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Storage & Handling
Storage
-20℃, dry, sealed
description Product Description
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds between aromatic systems. Its primary application lies in organic synthesis, particularly in the preparation of conjugated organic materials such as semiconductors, OLEDs, and pharmaceutical intermediates. The compound acts as a boronic ester derivative, offering enhanced stability and reactivity with halogenated arenes in the presence of palladium catalysts. It is especially valuable in the synthesis of thiophene-based functional molecules for electronic and optoelectronic devices.
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