CAS 214750-75-1
:N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-D-lysine
Description:
N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-D-lysine, with CAS number 214750-75-1, is a synthetic amino acid derivative characterized by the presence of a lysine backbone modified with two distinct protective groups. The fluorenylmethoxycarbonyl (Fmoc) group is commonly used in peptide synthesis for its stability under basic conditions and ease of removal under acidic conditions, making it a popular choice for protecting amino groups. The second modification, the propenyloxycarbonyl group, introduces a reactive vinyl moiety that can participate in further chemical reactions, such as polymerization or conjugation with other biomolecules. This compound is typically utilized in the field of peptide chemistry and drug development, where its unique functional groups allow for the synthesis of complex peptides and the exploration of new therapeutic agents. Its solubility, stability, and reactivity are influenced by the presence of these functional groups, making it a versatile building block in organic synthesis and medicinal chemistry.
Formula:C25H28N2O6
InChI:InChI=1S/C25H28N2O6/c1-2-15-32-24(30)26-14-8-7-13-22(23(28)29)27-25(31)33-16-21-19-11-5-3-9-17(19)18-10-4-6-12-20(18)21/h2-6,9-12,21-22H,1,7-8,13-16H2,(H,26,30)(H,27,31)(H,28,29)/t22-/m1/s1
InChI key:InChIKey=OJBNDXHENJDCBA-JOCHJYFZSA-N
SMILES:C(OC(N[C@H](CCCCNC(OCC=C)=O)C(O)=O)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:- (2R)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-6-(prop-2-enoxycarbonylamino)hexanoic acid
- <span class="text-smallcaps">D</span>-Lysine, N<sup>2</sup>-[(9H-fluoren-9-ylmethoxy)carbonyl]-N<sup>6</sup>-[(2-propen-1-yloxy)carbonyl]-
- <span class="text-smallcaps">D</span>-Lysine, N<sup>2</sup>-[(9H-fluoren-9-ylmethoxy)carbonyl]-N<sup>6</sup>-[(2-propenyloxy)carbonyl]-
- Fmoc-<span class="text-smallcaps">D</span>-Lys(Alloc)
- Fmoc-D-Lys(Alloc)-OH
- Fmoc-D-Lys(Aloc)-OH
- N<sup>2</sup>-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N<sup>6</sup>-[(2-propen-1-yloxy)carbonyl]-<span class="text-smallcaps">D</span>-lysine
- D-Lysine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-
- Fmoc-D-Lys(Alloc)
- N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-D-lysine
- D-Lysine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propenyloxy)carbonyl]-
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Found 7 products.
Nε-Allyloxycarbonyl-Nα-Fmoc-D-lysine, 95%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C25H28N2O6Purity:95%Molecular weight:452.51Fmoc-D-Lys(Aloc)-OH
CAS:<p>Bachem ID: 4027977.</p>Formula:C25H28N2O6Purity:99.47%Color and Shape:White PowderMolecular weight:452.51N-alpha-Fmoc-Nepsilon-allyloxycarbonyl-D-lysine
CAS:<p>N-alpha-Fmoc-Nepsilon-allyloxycarbonyl-D-lysine is a medicament that is modified with an amino group at the alpha position. It is synthesized by modification of the chain with a ganirelix acetate. N-alpha-Fmoc-Nepsilon-allyloxycarbonyl-D-lysine can be used to produce ganirelix, which inhibits the release of follicle stimulating hormone (FSH). The chemical synthesis of this drug has been shown to be successful in large scale production, and it has been shown to be effective in treating patients with prostate cancer. Impurities in this drug have been found and treated by removing the methyl ester group from the lysine residue.</p>Formula:C25H28N2O6Purity:Min. 95%Molecular weight:452.5 g/mol






