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Structure of 1153949-38-2
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This boronate-functionalized pyrazole derivative integrates a sterically hindered tetramethyl-1,3,2-dioxaborolane moiety with a nitrile-bearing cyclopentylpropyl linker, enabling efficient Suzuki-Miyaura cross-coupling under standard conditions. The robust boronate group withstands bench storage and facilitates modular assembly of complex heterocyclic architectures in medicinal chemistry and materials science applications.
3-Cyclopentyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]propanenitrile serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The pyrazole moiety provides robust heterocyclic functionality, while the nitrile group enables downstream transformations. Bench-stable and compatible with standard reaction conditions, it facilitates efficient construction of complex molecular architectures in medicinal chemistry and materials science applications.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: