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Structure of 389799-45-5
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(4-Chloropyrimidin-5-yl)methanol features a pyrimidine core bearing a chloro substituent at the 4-position and a primary alcohol at the 5-position. This combination enables direct functionalization in synthetic sequences, particularly in nucleophilic substitution reactions or as a linker for bioconjugation. The molecule exhibits good stability under standard bench conditions and facilitates integration into pharmaceutical intermediates and agrochemical scaffolds.
(4-Chloropyrimidin-5-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its chloro group facilitates nucleophilic substitution reactions, while the pendant alcohol supports derivatization via esterification or ether formation. The compound exhibits good bench stability and is compatible with standard coupling protocols, making it well-suited for modular synthesis of kinase inhibitors and other bioactive heterocycles.
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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: