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Structure of 106247-35-2
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2-Amino-4,4-dimethylpentanoic acid features a sterically hindered aliphatic backbone with a terminal carboxylic acid and primary amine group. This configuration supports stable peptide coupling under standard conditions, enabling efficient incorporation into bioactive sequences. The dimethyl substitution enhances resistance to racemization during activation.
2-Amino-4,4-dimethylpentanoic acid serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of amino acid derivatives and peptidomimetics. Its tert-butyl-substituted backbone provides steric hindrance and metabolic stability, while the amino and carboxylic acid functionalities offer versatile handles for coupling reactions and derivatization. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for use in solid-phase synthesis and API intermediate 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: