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Structure of 1798304-51-4
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This boronate moiety integrates a cyclopropyl-substituted pyrimidine scaffold, offering enhanced metabolic stability and favorable solubility. The methoxy group at C6 modulates electronic properties, enabling efficient coupling in Suzuki-Miyaura reactions under standard conditions. Designed for streamlined synthesis of bioactive heterocycles, this reagent delivers high functional group tolerance and bench-stable handling.
(4-Cyclopropyl-6-methoxypyrimidin-5-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. Its pyrimidine core provides enhanced metabolic stability and favorable physicochemical properties, while the cyclopropyl and methoxy substituents offer tunable steric and electronic profiles. The boronic acid moiety exhibits good bench stability and compatibility with diverse functional groups, facilitating straightforward purification and integration into complex molecular architectures common in medicinal chemistry and agrochemical research.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: