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Structure of 941294-36-6
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2-Chloro-4-isopropylpyrimidine features a chlorine substituent at the 2-position and a sterically hindered isopropyl group at the 4-position, delivering enhanced stability and selective reactivity. This electronic and steric profile enables efficient coupling in heterocyclic synthesis, particularly in medicinal chemistry applications requiring controlled functionalization of pyrimidine scaffolds.
2-Chloro-4-isopropylpyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. Its electrophilic chlorine atom at the 2-position exhibits high reactivity with nucleophiles under mild conditions, while the 4-isopropyl group provides steric and electronic modulation. The compound demonstrates excellent bench stability, ease of purification, and compatibility with diverse functional groups, making it a reliable scaffold for constructing bioactive heterocycles and API intermediates.
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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#: 2810
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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: