CAS 1191429-14-7

(2R)-8-Azido-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-methyloctanoic acid

Description:

(2R)-8-Azido-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-methyloctanoic acid is a synthetic organic compound characterized by its azido functional group, which is known for its reactivity and utility in click chemistry. The presence of the fluorenylmethoxycarbonyl (Fmoc) group indicates that this compound is likely used in peptide synthesis, serving as a protective group for amino acids. The structure features a branched octanoic acid backbone, which contributes to its hydrophobic characteristics, while the azido group introduces a polar functional group that can participate in various chemical reactions. This compound is typically utilized in biochemical applications, particularly in the development of pharmaceuticals and bioconjugation strategies. Its specific stereochemistry (2R) suggests that it has a defined spatial arrangement, which can influence its biological activity and interaction with other molecules. Overall, this compound exemplifies the intersection of organic synthesis and medicinal chemistry, showcasing the importance of functional groups in determining the reactivity and application of chemical substances.

Formula: C₂₄H₂₈N₄O₄

InChI: InChI=1S/C24H28N4O4/c1-24(22(29)30,14-8-2-3-9-15-26-28-25)27-23(31)32-16-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h4-7,10-13,21H,2-3,8-9,14-16H2,1H3,(H,27,31)(H,29,30)/t24-/m1/s1

InChI key: InChIKey=MSKNYBLJPSFPBR-XMMPIXPASA-N

SMILES: C(OC(N[C@](CCCCCCN=[N+]=[N-])(C(O)=O)C)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2

Synonyms:

• Octanoic acid, 8-azido-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-, (2R)-
• (2R)-8-Azido-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-methyloctanoic acid
• (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-8-azido-2-methyloctanoic acid