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Structure of 1000801-76-2
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This pyrazole derivative features a methoxypropyl group and a boronate ester moiety, enabling direct use in Suzuki-Miyaura cross-coupling reactions. The tetramethyl-substituted dioxaborolane enhances stability and reactivity under standard conditions, while the electron-rich pyrazole core facilitates efficient coupling with aryl halides. Designed for streamlined synthesis of complex heterocycles, this compound offers robust performance in diverse reaction environments.
1-(3-Methoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The pyrazole core provides metabolic stability and hydrogen-bonding capability, while the 3-methoxypropyl substituent enhances solubility and modulates lipophilicity. Bench-stable and compatible with diverse reaction conditions, it facilitates efficient construction of biaryl and heteroaryl scaffolds in medicinal chemistry and materials synthesis.
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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: