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Structure of 149709-59-1
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(R)-Ethyl 5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpent-2-enoate features a chiral α,β-unsaturated ester framework with a bulky biphenyl substituent and a protected amine. This bench-stable building block integrates readily into asymmetric synthesis workflows, enabling efficient access to complex biaryl-containing peptidomimetics and pharmaceutical intermediates under standard conditions.
(R)-Ethyl 5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpent-2-enoate serves as a versatile chiral building block for the synthesis of biologically relevant heterocycles and peptidomimetics. Its conjugated enoate moiety enables efficient Michael additions and Diels–Alder reactions, while the Boc-protected amine offers orthogonal handling. The molecule exhibits excellent bench stability, facilitates straightforward deprotection, and supports functional group tolerance in multi-step synthetic sequences.
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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: