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CAS 327156-94-5

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N-α-Boc-N-ε-allyloxycarbonyl-D-lysine dicyclohexylamine salt

Description:
N-α-Boc-N-ε-allyloxycarbonyl-D-lysine dicyclohexylamine salt is a chemical compound that serves as a protected form of the amino acid D-lysine, which is essential in various biochemical applications, particularly in peptide synthesis. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group used to shield the amino group during chemical reactions, while the "allyloxycarbonyl" moiety provides additional protection and can facilitate further functionalization. The presence of dicyclohexylamine as a counterion indicates that the compound is a salt, which can influence its solubility and stability. This compound is typically utilized in organic synthesis and medicinal chemistry, where the protection of functional groups is crucial for the selective modification of amino acids. Its characteristics include a relatively high molecular weight, specific solubility in organic solvents, and stability under standard laboratory conditions. As with many chemical substances, proper handling and safety precautions are essential due to potential reactivity and toxicity.
Formula:C27H49N3O6
InChI:InChI=1/C15H26N2O6.C12H23N/c1-5-10-22-13(20)16-9-7-6-8-11(12(18)19)17-14(21)23-15(2,3)4;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h5,11H,1,6-10H2,2-4H3,(H,16,20)(H,17,21)(H,18,19);11-13H,1-10H2/t11-;/m1./s1
SMILES:C=CCOC(=NCCCC[C@H](C(=O)O)N=C(O)OC(C)(C)C)O.C1CCC(CC1)NC1CCCCC1
Synonyms:
  • Boc-d-lys(alloc)-oh dcha
  • Boc-d-lys(alloc)-oh dicyclohexylamine salt
  • Boc-d-lys(aloc)-oh dcha
  • Boc-d-lysine allyl ester dcha salt
  • Boc-n-epsilon-allyloxycarbonyl-d-lysine dicyclohexyl ammonium salt
  • ndelta-alloc-nalpha-Boc-d-lysine dicyclohexylamine salt
  • nalpha-Boc-ndelta-alloc-d-lysine dicyclohexylamine salt
  • N-Alpha-Tert-Butyloxycarbonyl-N-Epsilon-Allyloxycarbonyl-D-Lysine Dicyclohexylamine
  • N~2~-(tert-butoxycarbonyl)-N~6~-[(prop-2-en-1-yloxy)carbonyl]-D-lysine-N-cyclohexylcyclohexanamine (1:1)
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