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Structure of 34953-87-2
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(2-Chloropyrimidin-4-yl)methanol features a reactive chloropyrimidine core paired with a primary alcohol handle, enabling direct functionalization in nucleophilic substitution or coupling workflows. This bench-stable, moisture-tolerant reagent integrates efficiently into heterocyclic synthesis, serving as a key building block for pharmaceutical intermediates and bioactive molecule scaffolds.
(2-Chloropyrimidin-4-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient introduction of the pyrimidine scaffold into target molecules. Its chloro group facilitates nucleophilic substitution reactions, while the pendant alcohol supports derivatization or protection strategies. The compound exhibits good bench stability and is compatible with standard synthetic workflows, making it well-suited for the construction of heterocyclic intermediates and API candidates.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: