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Structure of 1290191-64-8
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tert-Butyl N-[(1R,3R)-3-hydroxycyclopentyl]carbamate features a chiral cyclopentane scaffold bearing a hydroxyl group and a carbamate protecting group. This configuration enables selective functionalization in asymmetric synthesis, where the hydroxyl moiety serves as a handle for derivatization under mild conditions. The tert-butyl carbamate offers stability during reaction sequences and can be removed cleanly when required.
tert-Butyl N-[(1R,3R)-3-hydroxycyclopentyl]carbamate serves as a versatile chiral building block in synthetic organic chemistry, enabling stereoselective transformations via its protected amine and pendant hydroxyl group. The (1R,3R)-configured cyclopentane ring provides a rigid scaffold for conformationally constrained libraries, while the tert-butoxycarbonyl (Boc) group offers excellent bench stability and facile deprotection under mild acidic conditions. This compound facilitates efficient functionalization at both nitrogen and carbon centers, supporting diverse downstream applications in medicinal chemistry and natural product 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: