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Structure of 49607-08-1
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(S)-2-Amino-2-cyclobutylacetic acid features a chiral cyclobutyl group that imparts distinct stereochemical control in peptide synthesis. This bench-stable amino acid derivative integrates readily into peptidomimetics, offering enhanced conformational rigidity and metabolic stability. The cyclobutyl moiety provides unique steric and electronic properties beneficial for targeting bioactive conformations in drug discovery.
(S)-2-Amino-2-cyclobutylacetic acid serves as a valuable chiral building block for the synthesis of bioactive molecules, particularly in medicinal chemistry and peptide-based drug discovery. Its cyclobutyl substituent imparts distinct conformational rigidity, enabling precise control over molecular geometry. The molecule exhibits excellent bench stability, facilitates straightforward purification, and demonstrates compatibility with standard amino acid coupling protocols. Functions as a key scaffold in the development of targeted therapeutics.
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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: