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Structure of 1025351-41-0
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(6-Chloropyrimidin-4-yl)methanol features a pyrimidine core functionalized with a chlorine atom at the 6-position and a methanol group at the 4-position, enabling direct coupling in nucleophilic substitution reactions. This bench-stable derivative serves as a key building block for medicinal chemistry, particularly in the synthesis of kinase inhibitors and antiviral agents, where its electron-deficient heterocycle enhances reactivity and target affinity.
(6-Chloropyrimidin-4-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds through nucleophilic substitution and coupling reactions. Its bench-stable nature and compatibility with diverse functional groups facilitate straightforward incorporation into target molecules. The chloro substituent provides a reliable handle for further derivatization, while the alcohol functionality supports orthogonal transformations, making it a practical choice for modular synthesis of bioactive compounds.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: