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Structure of 142217-81-0
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This purine derivative features a uniquely functionalized cyclopentyl scaffold bearing benzyl ether and methylene groups, enabling precise spatial control in nucleoside analog synthesis. The amino-purine core integrates readily into bioactive heterocycles, while the benzyloxy substituents provide orthogonal protection for downstream transformations under standard conditions.
2-Amino-9-((1S,3R,4S)-4-(benzyloxy)-3-((benzyloxy)methyl)-2-methylenecyclopentyl)-1H-purin-6(9H)-one serves as a key purine scaffold for medicinal chemistry exploration, featuring orthogonal benzyl protecting groups that enable selective deprotection and functionalization. Its stable cyclopentyl core facilitates modular derivatization, while the amino and carbonyl functionalities support standard coupling and transformation protocols in nucleoside analog synthesis.
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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: