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CAS 1025796-31-9

:

1,5-Bis(1,1-dimethylethyl) N-[[[(1S)-5-amino-1-[(1,1-dimethylethoxy)carbonyl]pentyl]amino]carbonyl]-L-glutamate

Description:
1,5-Bis(1,1-dimethylethyl) N-[[[(1S)-5-amino-1-[(1,1-dimethylethoxy)carbonyl]pentyl]amino]carbonyl]-L-glutamate, identified by CAS number 1025796-31-9, is a complex organic compound characterized by its multi-functional structure. It features a glutamate backbone, which is an amino acid known for its role in protein synthesis and neurotransmission. The presence of multiple tert-butyl groups (1,1-dimethylethyl) contributes to its hydrophobic characteristics, potentially influencing its solubility and interaction with biological membranes. The compound also contains an amino group and a carbonyl group, which are indicative of its potential reactivity and ability to form peptide bonds. This structure suggests that it may have applications in biochemistry, particularly in drug design or as a biochemical probe, due to its ability to mimic natural substrates or ligands. Overall, the compound's unique combination of hydrophobic and polar functional groups may allow for diverse interactions in biological systems.
Formula:C24H45N3O7
InChI:InChI=1S/C24H45N3O7/c1-22(2,3)32-18(28)14-13-17(20(30)34-24(7,8)9)27-21(31)26-16(12-10-11-15-25)19(29)33-23(4,5)6/h16-17H,10-15,25H2,1-9H3,(H2,26,27,31)/t16-,17-/m0/s1
InChI key:InChIKey=IXWXFSGSTGXUFO-IRXDYDNUSA-N
SMILES:[C@H](NC(N[C@H](C(OC(C)(C)C)=O)CCCCN)=O)(CCC(OC(C)(C)C)=O)C(OC(C)(C)C)=O
Synonyms:
  • 1,5-Bis(1,1-dimethylethyl) N-[[[(1S)-5-amino-1-[(1,1-dimethylethoxy)carbonyl]pentyl]amino]carbonyl]-L-glutamate
  • L-Glutamic acid, N-[[[(1S)-5-amino-1-[(1,1-dimethylethoxy)carbonyl]pentyl]amino]carbonyl]-, 1,5-bis(1,1-dimethylethyl) ester
  • Di-tert-butyl (((S)-6-amino-1-(tert-butoxy)-1-oxohexan-2-yl)carbamoyl)-L-glutamate
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