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Structure of 13433-00-6
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Diethyl aminomalonate hydrochloride serves as a stabilized, bench-ready synthon for C–C bond formation. The protonated amine enhances solubility and reactivity in polar media, enabling efficient enolate generation under mild conditions. This derivative integrates seamlessly into multistep sequences requiring nitrogen-tethered malonate equivalents, delivering high functional group tolerance and predictable regiochemistry in asymmetric synthesis workflows.
Diethyl aminomalonate hydrochloride serves as a versatile building block in synthetic organic chemistry, enabling the efficient construction of β-amino carbonyl compounds and heterocyclic scaffolds. Its stabilized enolizable α-position facilitates nucleophilic additions and condensation reactions, while the protonated amine enhances solubility and handling. The salt form improves bench stability and simplifies purification, making it well-suited for multi-step syntheses and scale-up applications.
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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: