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Structure of 123367-26-0
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Selectively protected building block for library synthesis or the preparation of -glutamyl peptides by Fmoc SPPS. After condensation of the side-chain carboxy with an appropriate amine or alcohol, the -amino and carboxy functions can be selectively unmasked with 20% piperidine in DMF and 50% TFA in DCM respectively, facilitating the synthesis of branched esters, amides, lactams and lactones containing the glutamyl unit. Associated Protocols and Technical ArticlesCleavage and Deprotection Protocols for Fmoc SPPS
(E)-3-(Dimethylamino)-1-(pyridin-3-yl)prop-2-en-1-one serves as a versatile enaminone building block in synthetic organic chemistry, enabling efficient access to nitrogen-containing heterocycles and conjugated systems. Its extended π-conjugation and electron-rich dimethylamino group facilitate electrophilic substitution and Michael addition reactions under mild conditions. The compound exhibits bench stability, ease of purification, and compatibility with diverse functional groups, making it valuable for medicinal chemistry lead optimization and macrocyclic scaffold construction.
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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-H332-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: