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Thank you very much for your interest in our products. All prices listed on our website are ex-works, Germany, and may attract customs duties when imported.
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Continue to Iris Biotech GmbHSend request to US distributorChemischer Name: (S)-2-(Fmoc-amino)-6-(Boc-aminoxy)hexanoic acid // Synonyme: (S)-Fmoc-AAHA(Boc)-OH, Fmoc-(S)-AAHA(Boc)-OH, Fmoc-AAHA(Boc)-OH, (N-alpha-(9-Fluorenylmethyloxycarbonyl)-amino)-6-((t-butyloxycarbonyl)-aminooxy)hexanoic acid,(S)-2-((((9H-fluoren-9-yl)methoxy)carbo nyl)amino)-6-(((tert-butoxycarbonyl)amino)oxy)hexa
Ab 175,00 €
The aminooxy group exhibits greater nucleophilicity than the corresponding primary amino group. It is therefore considered to react chemoselectively with carbonyl compounds by forming a kinetically stable oxime bond, which is more stable than an imine bond.
Synthesis of (S)-(+)-2-Amino-6-(Aminooxy)-hexanoic acid; M. Adamczyk, R. E. Reddy; Synth. Commun. 2001; 31: 579-586. https://doi.org/10.1081/SCC-100000585.
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