2-(2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethyl)isoindoline-1,3-dione
96%
Reagent
Code: #243618
CAS Number
957061-09-5
blur_circular Chemical Specifications
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Molecular Information
Weight
393.2 g/mol
Formula
C₂₂H₂₄BNO₅
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Registry Numbers
MDL Number
MFCD09258656
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Storage & Handling
Storage
2-8°C, dry
description Product Description
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the preparation of complex organic molecules, including pharmaceuticals and functional materials. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development. Its phthalimide moiety can be deprotected to release amines, allowing further functionalization in multi-step syntheses. Commonly employed in the construction of biaryl systems, it supports the creation of advanced intermediates for agrochemicals, OLED materials, and bioactive compounds.
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