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Structure of 1068435-19-7
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a reactive pentenyl handle and an extended enoic acid chain, enabling efficient conjugation in peptide synthesis. The fluorenylmethoxycarbonyl group ensures stable protection under standard conditions, while the pendant alkene functionalities facilitate post-functionalization via click chemistry or polymer coupling.
2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(pent-4-en-1-yl)hept-6-enoic acid serves as a versatile bifunctional building block in peptide synthesis and medicinal chemistry, combining a robust Fmoc protecting group with a terminal alkyne and α,β-unsaturated carbonyl system. Its stability under standard coupling conditions enables efficient incorporation into complex scaffolds, while the pendant alkene and alkyne functionalities facilitate post-coupling modifications via click chemistry or conjugate addition.
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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: