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Structure of 367278-49-7
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(R)-3-Amino-4,4-dimethylpentanoic acid is a chiral building block featuring a sterically hindered α-amino acid scaffold. The geminal dimethyl groups enhance metabolic stability and influence conformational rigidity, while the primary amine and carboxylic acid functionalities enable direct incorporation into peptide sequences or conjugation workflows under standard conditions.
(R)-3-Amino-4,4-dimethylpentanoic acid serves as a valuable chiral building block for peptide-based drug discovery and asymmetric synthesis. Its tertiary α-carbon enhances metabolic stability, while the pendant amine and carboxylic acid enable diverse functionalization via standard coupling, acylation, and cyclization protocols. The compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for iterative synthetic workflows in medicinal chemistry and process development.
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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: