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Structure of 7306-68-5
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6-Chloro-9-(2-tetrahydropyranyl)purine serves as a protected purine scaffold for nucleoside synthesis, featuring a labile tetrahydropyranyl group at the 9-position. This protecting group enables selective functionalization under mild conditions while maintaining stability during standard reaction protocols. The chloro substituent at C6 imparts enhanced reactivity in cross-coupling processes and facilitates downstream derivatization.
6-Chloro-9-(2-tetrahydropyranyl)purine serves as a versatile purine scaffold for medicinal chemistry and heterocyclic synthesis. The 6-chloro group enables nucleophilic substitution reactions, while the 2-tetrahydropyranyl protecting group ensures stability and orthogonality during multi-step transformations. This compound facilitates efficient access to functionalized purine derivatives with enhanced solubility and handling characteristics, making it ideal for iterative synthetic campaigns in drug discovery.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: