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Structure of 177269-37-3
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Methyl 3-amino-2,2-dimethylpropanoate hydrochloride features a sterically hindered quaternary carbon center and a protonated primary amine, enhancing solubility and stability in protic solvents. This bench-stable derivative facilitates efficient coupling reactions in peptide synthesis and medicinal chemistry workflows.
Methyl 3-amino-2,2-dimethylpropanoate hydrochloride serves as a versatile building block in medicinal chemistry, enabling the synthesis of sterically hindered amino acid analogs and heterocyclic scaffolds. Its tertiary α-carbon prevents racemization during peptide coupling, while the protonated amine enhances solubility and facilitates purification. The ester group supports subsequent transformations such as hydrolysis or nucleophilic substitution, making it ideal for robust, scalable synthetic routes.
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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: