2-(Thiophen-2-yl)-1,3,2-dioxaborinane
97%
Reagent
Code: #243436
CAS Number
197024-83-2
blur_circular Chemical Specifications
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Molecular Information
Weight
168.02 g/mol
Formula
C₇H₉BO₂S
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Registry Numbers
MDL Number
MFCD11053858
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Storage & Handling
Storage
-20°C, light-proof, inert gas
description Product Description
Used in organic synthesis as a boronic ester reagent for Suzuki-Miyaura cross-coupling reactions. It enables the formation of carbon-carbon bonds, particularly in the construction of biaryl and heteroaryl compounds, which are common scaffolds in pharmaceuticals and agrochemicals. The thiophene moiety enhances electronic and structural properties, making it valuable in materials science for developing conjugated systems in organic electronics such as OLEDs and semiconducting polymers. Its stability and reactivity profile allow for selective transformations under mild conditions, useful in late-stage functionalization of complex molecules.
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