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Structure of 21254-22-8
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4,6-Dichloro-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidine features a sterically hindered isopropyl group and electron-deficient pyrazolopyrimidine core, enabling selective coupling in kinase inhibitor scaffolds. This bench-stable heterocycle integrates readily into medicinal chemistry campaigns requiring halogen-directed functionalization under standard conditions.
4,6-Dichloro-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of purine-like scaffolds via nucleophilic substitution. The dichloro functionality provides orthogonal reactivity for sequential functionalization, while the isopropyl group enhances solubility and stability. This compound facilitates rapid diversification in kinase inhibitor and antiviral agent development, offering reliable performance in standard coupling protocols and robust bench handling.
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GHS Pictogram :
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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-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P405-P501
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Lot numbers can be found on the outside label of a product: