Peptides & Peptide Synthesis Products

Fmoc-Cys(Trt)-OH

Fmoc-Cys(Trt)-OH

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Fmoc-Cys(Trt)-OH, Catalog No: 41008
Nα-Fmoc-S-trityl-L-cysteine, CAS: 103213-32-7, MW: 585.71, Formula: C37H31NO4S
Catalog No: 41008
Nα-Fmoc-S-trityl-L-cysteine, CAS: 103213-32-7, MW: 585.71, Formula: C37H31NO4S

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Description

Details

Nα-Fmoc-S-trityl-L-cysteine
Additional Information

Additional Information

Catalog Number 41008
CAS 103213-32-7
M.W. 585.71
Formula C37H31NO4S
IUPAC Name (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanylpropanoic acid
Synonym Nα-Fmoc-S-trityl-L-cysteine
Also Known As
  • (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[tri(phenyl)methylsulfanyl]propanoic acid
  • (2R)-2-[(9H-fluoren-9-ylmethoxy-oxomethyl)amino]-3-[tri(phenyl)methylthio]propanoic acid
  • (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[tri(phenyl)methylthio]propionic acid
  • Nalpha-Fmoc-S-trityl-L-cysteine
  • 08503_FLUKA
  • Fmoc-D-Cys(Trt)-OH
  • Nalpha-Fmoc-S-trityl-D-cysteine
  • Fmoc-S-trityl-cys
  • L-Cysteine, N-((9H-fluoren-9-ylmethoxy)carbonyl)-S-(triphenylmethyl)-
  • N(alpha)-Fluorenylmethyloxycarbonyl-S-tritylcysteine
  • 47695_FLUKA
  • Fmoc-Cys(Trt)-OH
  • N-(9-Fluorenylmethoxycarbonyl)-S-trityl-L-cysteine
InChIKey KLBPUVPNPAJWHZ-UMSFTDKQSA-N
InChI InChI=1S/C37H31NO4S/c39-35(40)34(38-36(41)42-24-33-31-22-12-10-20-29(31)30-21-11-13-23-32(30)33)25-43-37(26-14-4-1-5-15-26,27-16-6-2-7-17-27)28-18-8-3-9-19-28/h1-23,33-34H,24-25H2,(H,38,41)(H,39,40)/t34-/m0/s1
SMILES C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)SC[C@@H](C(=O)O)NC(=O)OCC4C5=CC=CC=C5C6=CC=CC=C46
Cited Uses

Details

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12. Huang J et al, "Residue analysis of a CTL epitope of SARS-CoV spike protein by IFN-gamma production and bioinformatics prediction", BMC Immunology, 13() pp.50 ().
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14. Tatsi A et al, "[111In-DOTA]Somatostatin-14 analogs as potential pansomatostatin-like radiotracers - first results of a preclinical study", EJNMMI Research, 2() pp.25 ().
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19. Lin CC et al, "PEG hydrogels formed by thiol-ene photo-click chemistry and their effect on the formation and recovery of insulin-secreting cell spheroids", Biomaterials, 32(36) pp.9685-9695 (2011 Dec).
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22. Nefzi A et al, "N-terminus 4-Chloromethyl Thiazole Peptide as a Macrocyclization Tool in the Synthesis of Cyclic Peptides: Application to the Synthesis of Conformationally Constrained RGD-Containing Integrin Ligands", Tetrahedron letters, 52(7) pp.817-819 (2011 Feb 16).
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