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CAS 208522-16-1

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(2S)-2-[(tert-butoxycarbonyl)amino]hex-5-ynoic acid

Description:
(2S)-2-[(tert-butoxycarbonyl)amino]hex-5-ynoic acid is an amino acid derivative characterized by its unique structure, which includes a hexynoic acid backbone with a tert-butoxycarbonyl (Boc) protecting group on the amino functional group. This compound features a chiral center at the second carbon, denoted by the (2S) configuration, indicating its specific stereochemistry. The presence of the alkyne functional group (hex-5-ynoic acid) contributes to its reactivity, making it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and biologically active compounds. The Boc group serves as a protective moiety, allowing for selective reactions at other functional groups without interference. This compound is typically soluble in organic solvents and may exhibit moderate solubility in water, depending on the pH. Its properties, such as melting point and boiling point, can vary based on purity and environmental conditions. Overall, (2S)-2-[(tert-butoxycarbonyl)amino]hex-5-ynoic acid is significant in synthetic organic chemistry for its versatility and functional group compatibility.
Formula:C11H17NO4
InChI:InChI=1/C11H17NO4/c1-5-6-7-8(9(13)14)12-10(15)16-11(2,3)4/h1,8H,6-7H2,2-4H3,(H,12,15)(H,13,14)/t8-/m0/s1
SMILES:C#CCC[C@@H](C(=O)O)N=C(O)OC(C)(C)C
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