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Structure of 98141-42-5
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4,6-Dichloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidine features a fused pyrazolopyrimidine core with two chlorine substituents at electron-deficient positions, enabling selective functionalization in transition-metal-catalyzed cross-coupling reactions. The methyl group enhances solubility and stability under standard conditions, while the dichloro substitution pattern facilitates efficient incorporation into bioactive scaffolds. This compound serves as a key intermediate for pharmaceutical and agrochemical development.
4,6-Dichloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of purine-like scaffolds. The dichloro substitution pattern facilitates nucleophilic aromatic substitution under mild conditions, allowing for selective derivatization at C4 and C6 positions. Its bench-stable crystalline form and compatibility with diverse functional groups make it ideal for parallel synthesis campaigns targeting kinase inhibitors and antiviral agents.
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: