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CAS 115109-65-4

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5-[3,5-DIMETHOXY-4-(FMOC-AMINOMETHYL)PHENOXY]PENTANOIC ACID

Description:
5-[3,5-Dimethoxy-4-(FMOC-aminomethyl)phenoxy]pentanoic acid, with the CAS number 115109-65-4, is a chemical compound characterized by its complex structure that includes a pentanoic acid backbone and a phenoxy group substituted with dimethoxy and FMOC (fluorenylmethyloxycarbonyl) functionalities. The presence of the FMOC group indicates that this compound is likely used in peptide synthesis, serving as a protective group for amines. The dimethoxy substitutions on the phenyl ring enhance the compound's lipophilicity and may influence its reactivity and interaction with biological systems. This compound is typically utilized in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. Its unique structural features suggest potential applications in drug design, where modifications can lead to variations in biological activity. As with many organic compounds, its solubility, stability, and reactivity will depend on the specific conditions under which it is handled, including solvent choice and temperature.
Formula:C29H31NO7
InChI:InChI=1/C29H31NO7/c1-34-26-15-19(36-14-8-7-13-28(31)32)16-27(35-2)24(26)17-30-29(33)37-18-25-22-11-5-3-9-20(22)21-10-4-6-12-23(21)25/h3-6,9-12,15-16,25H,7-8,13-14,17-18H2,1-2H3,(H,30,33)(H,31,32)
InChI key:ATYUCXIJDKHOPX-UHFFFAOYSA-N
SMILES:COc1cc(cc(c1CN=C(O)OCC1c2ccccc2c2ccccc12)OC)OCCCCC(=O)O
Synonyms:
  • 5-(4-(9-Fluorenylmethyloxycarbonyl)Aminomethyl-3,5-Dimethoxyphenoxy)Valericaci
  • N-Fmoc-Pal Linker
  • Pal Linker
  • Fmoc-Pal-Linker
  • 5-[4-[(9-Fluorenylmethoxy)Aminomethyl]-3,5-Dimethoxyphenoxy]-Pentanoic Acid
  • 5-[4-(9-Fluorenylmethoxycarbonyl)Aminomethyl-3,5-Dimethoxyphenoxy]-Pentanoic Acid
  • 5-(4-N-Fmoc-Aminomethyl-3,5-Dimethoxyphenoxy)Pentanoic Acid
  • 5-[4-({[(9H-fluoren-9-ylmethoxy)carbonyl]amino}methyl)-3,5-dimethoxyphenoxy]pentanoic acid
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