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CAS 159751-47-0

:

Fmoc-L-.alpha.-aminoadipic acid-delta-t-butyl ester

Description:
Fmoc-L-α-aminoadipic acid-delta-t-butyl ester is a synthetic compound commonly used in peptide synthesis and research. It features a protected amino acid structure, where the Fmoc (9-fluorenylmethoxycarbonyl) group serves as a temporary protective group for the amino functionality, facilitating selective reactions during peptide assembly. The delta-t-butyl ester moiety provides additional protection for the carboxylic acid group, enhancing the compound's stability and solubility in organic solvents. This compound is characterized by its ability to participate in coupling reactions, making it valuable in the synthesis of peptides and other complex organic molecules. Its structure includes a six-carbon chain (adipic acid) with an amino group, contributing to its role in forming peptide bonds. The presence of the Fmoc group allows for easy removal under mild basic conditions, enabling the subsequent formation of peptide bonds. Overall, Fmoc-L-α-aminoadipic acid-delta-t-butyl ester is an important intermediate in the field of organic chemistry and biochemistry, particularly in the development of pharmaceuticals and biologically active compounds.
Formula:C25H29NO6
InChI:InChI=1/C25H29NO6/c1-25(2,3)32-22(27)14-8-13-21(23(28)29)26-24(30)31-15-20-18-11-6-4-9-16(18)17-10-5-7-12-19(17)20/h4-7,9-12,20-21H,8,13-15H2,1-3H3,(H,26,30)(H,28,29)/t21-/m0/s1
SMILES:CC(C)(C)OC(=O)CCC[C@@H](C(=O)O)N=C(O)OCC1c2ccccc2c2ccccc12
Synonyms:
  • 6-tert-butoxy-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-6-oxo-L-norleucine
  • Fmoc-Aad(Otbu)-Oh
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