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CAS 276869-41-1

:

(2S)-8-tert-butoxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)-8-oxo-octanoic acid

Description:
(2S)-8-tert-butoxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)-8-oxo-octanoic acid is a synthetic organic compound characterized by its complex structure, which includes a tert-butoxy group, a fluorenylmethoxycarbonyl (Fmoc) protecting group, and an octanoic acid backbone. This compound features a chiral center at the second carbon, contributing to its stereochemistry. The presence of the oxo group indicates that it has a ketone functional group, which can influence its reactivity and interactions. The Fmoc group is commonly used in peptide synthesis as a protective group for amino acids, allowing for selective reactions. The tert-butoxy group enhances the lipophilicity of the molecule, potentially affecting its solubility and permeability in biological systems. Overall, this compound is likely to be of interest in medicinal chemistry and peptide synthesis due to its structural features and functional groups, which may facilitate various chemical reactions and applications in drug development.
Formula:C27H33NO6
InChI:InChI=1/C27H33NO6/c1-27(2,3)34-24(29)16-6-4-5-15-23(25(30)31)28-26(32)33-17-22-20-13-9-7-11-18(20)19-12-8-10-14-21(19)22/h7-14,22-23H,4-6,15-17H2,1-3H3,(H,28,32)(H,30,31)/t23-/m0/s1
SMILES:CC(C)(C)OC(=O)CCCCC[C@@H](C(=O)O)N=C(O)OCC1c2ccccc2c2ccccc12
Synonyms:
  • (S)-2-FMOC-Amino-octanedioic acid 8-tert-butyl ester
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