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CAS 507472-26-6

:

(βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-nitrobenzenepropanoic acid

Description:
The chemical substance known as (βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-nitrobenzenepropanoic acid, with the CAS number 507472-26-6, is a synthetic compound primarily used in peptide synthesis and as a protecting group in organic chemistry. This compound features a fluorenylmethoxycarbonyl (Fmoc) group, which is commonly employed to protect amino groups during peptide synthesis, allowing for selective deprotection under mild conditions. The presence of a nitro group on the aromatic ring contributes to its electronic properties, potentially influencing reactivity and solubility. The β-amino acid structure provides unique steric and electronic characteristics, making it valuable in the design of bioactive peptides and pharmaceuticals. Its chirality, indicated by the (βR) designation, suggests that it may exhibit specific interactions in biological systems, which can be critical for its function in medicinal chemistry. Overall, this compound exemplifies the intersection of organic synthesis and pharmaceutical applications, showcasing the importance of functional groups in determining chemical behavior and utility.
Formula:C24H20N2O6
InChI:InChI=1S/C24H20N2O6/c27-23(28)13-22(15-9-11-16(12-10-15)26(30)31)25-24(29)32-14-21-19-7-3-1-5-17(19)18-6-2-4-8-20(18)21/h1-12,21-22H,13-14H2,(H,25,29)(H,27,28)/t22-/m1/s1
InChI key:InChIKey=ODIITDVCGARGIW-JOCHJYFZSA-N
SMILES:C(OC(N[C@H](CC(O)=O)C1=CC=C(N(=O)=O)C=C1)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • (βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-nitrobenzenepropanoic acid
  • Benzenepropanoic acid, β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-nitro-, (βR)-
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