4,4,5,5-Tetramethyl-2-(oct-1-en-1-yl)-1,3,2-dioxaborolane
≥95%
Reagent
Code: #244101
CAS Number
170942-79-7
blur_circular Chemical Specifications
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Molecular Information
Weight
238.18 g/mol
Formula
C₁₄H₂₇BO₂
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Registry Numbers
MDL Number
MFCD03453667
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Storage & Handling
Storage
2-8°C, sealed, dry, inert gas
description Product Description
Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boron-based coupling partner to introduce alkenyl groups into aromatic or heteroaromatic systems, enabling the formation of carbon-carbon bonds. The presence of the oct-1-enyl chain allows for further functionalization or incorporation of long hydrophobic segments in target molecules, making it valuable in the synthesis of specialty organic compounds, including intermediates for pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity profile make it suitable for use in both laboratory-scale and industrial applications where selective and efficient coupling is required.
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