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670642 Sigma-Aldrich

Fmoc-Pen(Trt)-OH

96%

Synonym: Fmoc-β,β-dimethyl-Cys(Trt)-OH, Fmoc-S-trityl-L-penicillamine

  • CAS Number 201531-88-6

  • Empirical Formula (Hill Notation) C39H35NO4S

  • Molecular Weight 613.76

  •  MDL number MFCD00237388

  •  PubChem Substance ID 329760378

  •  NACRES NA.26

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Properties

Related Categories Chemical Biology, Chemical Synthesis, Penicillamine Derivatives, Peptide Synthesis and Peptide Chemistry, Unnatural Amino Acids & Derivatives More...
assay   ≥95.5% (HPLC)
  96%
optical activity   [α]/D +33±2°, c = 1 in methanol
storage temp.   2-8°C
SMILES string   CC(C)(SC(c1ccccc1)(c2ccccc2)c3ccccc3)[C@H](NC(=O)OCC4c5ccccc5-c6ccccc46)C(O)=O
InChI   1S/C39H35NO4S/c1-38(2,45-39(27-16-6-3-7-17-27,28-18-8-4-9-19-28)29-20-10-5-11-21-29)35(36(41)42)40-37(43)44-26-34-32-24-14-12-22-30(32)31-23-13-15-25-33(31)34/h3-25,34-35H,26H2,1-2H3,(H,40,43)(H,41,42)/t35-/m1/s1
InChI key   XSGMGAINOILNJR-PGUFJCEWSA-N

Description

Packaging

500 mg in poly bottle

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis (COA)

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Protocols & Articles

Articles

Unnatural Amino Acids - ChemFiles 2008, 8.7, 3.

Unnatural amino acids, the non-proteinogenic amino acids that either occur naturally or are chemically synthesized, are becoming more and more important as tools for modern drug discovery research. D...
Matthias Junkers
ChemFiles 2008, 8.7, 3.
Keywords: Absorption, Addition reactions, Alkylations, Asymmetric synthesis, Building blocks, Degradations, Drug discovery, Metabolism, Molecular probes, Peptidomimetics, Pharmaceutical

Peer-Reviewed Papers
15

References

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