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Structure of 1092938-92-5
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This boronate ester features a methoxycyclohexenyl moiety attached to a stable tetramethyl-1,3,2-dioxaborolane ring, enabling efficient Suzuki-Miyaura coupling under mild conditions. The electron-rich cyclohexenyl unit enhances reactivity, while the bulky tetramethyl substitution ensures excellent shelf life and resistance to protodeboronation. Ideal for constructing complex molecular architectures in synthetic and medicinal chemistry workflows.
2-(4-Methoxycyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. The cyclohexenyl moiety provides a rigid, electron-rich aryl equivalent with predictable regiochemistry, while the tetramethyl-substituted dioxaborolane enhances air and moisture stability. Its methoxy group offers orthogonal functionalization potential and improves solubility in common organic solvents, facilitating efficient coupling and straightforward purification.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: