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CAS 209252-16-4

:

(βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]benzenebutanoic acid

Description:
The chemical substance known as (βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]benzenebutanoic acid, with the CAS number 209252-16-4, is a synthetic compound primarily used in peptide synthesis and as a protecting group in organic chemistry. It features a fluorenylmethoxycarbonyl (Fmoc) group, which is commonly employed to protect amino groups during peptide synthesis due to its stability under basic conditions and ease of removal under acidic conditions. The compound has a chiral center, indicated by the (βR) designation, which contributes to its stereochemical properties and potential biological activity. Its structure includes a benzenebutanoic acid moiety, which may influence its solubility and interaction with biological systems. The presence of the fluorenyl group enhances its photophysical properties, making it useful in various applications, including drug development and materials science. Overall, this compound exemplifies the intersection of organic synthesis and medicinal chemistry, showcasing the importance of protecting groups in the synthesis of complex molecules.
Formula:C25H23NO4
InChI:InChI=1S/C25H23NO4/c27-24(28)15-18(14-17-8-2-1-3-9-17)26-25(29)30-16-23-21-12-6-4-10-19(21)20-11-5-7-13-22(20)23/h1-13,18,23H,14-16H2,(H,26,29)(H,27,28)/t18-/m1/s1
InChI key:InChIKey=DQNUGHJJKNFCND-GOSISDBHSA-N
SMILES:C(OC(N[C@H](CC1=CC=CC=C1)CC(O)=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • (3R)-3-([[(9H-Fluoren-9-yl)methoxy]carbonyl]amino)-4-phenylbutanoic acid
  • (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylbutyric acid
  • (R)-3-(9H-Fluoren-9-ylmethoxycarbonylamino)-4-phenylbutyric acid
  • (R)-3-(Fmoc-amino)-4-phenylbutyric acid
  • (βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]benzenebutanoic acid
  • 3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-phenylbutanoic acid
  • Benzenebutanoic acid, β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,(βR)-
  • Fmoc-D-β-HoPhe-OH
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