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47695 Aldrich

Fmoc-Cys(Trt)-OH

≥95.0% (sum of enantiomers, HPLC)

Synonym: N-(9-Fluorenylmethoxycarbonyl)-S-trityl-L-cysteine, Nα-Fmoc-S-trityl-L-cysteine

  • CAS Number 103213-32-7

  • Empirical Formula (Hill Notation) C37H31NO4S

  • Molecular Weight 585.71

  •  Beilstein Registry Number 4221286

  •  MDL number MFCD00038538

  •  PubChem Substance ID 57651084

  •  eCl@ss 32160406

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Properties

Related Categories Amino Acids & Derivatives, Chemical Biology, Chemical Synthesis, Cysteine/Cystine, Peptide Chemistry,
InChI Key   KLBPUVPNPAJWHZ-UMSFTDKQSA-N
assay   ≥95.0% (sum of enantiomers, HPLC)
optical activity   [α]20/D +16.0±2°, c = 1% in THF
mp   170-173 °C(lit.)
storage temp.   2-8°C

Description

Packaging

5 g in glass bottle

Price and Availability

Suggested Laboratory Gloves


Laboratory GlovesThis substance has been tested against several types of hand protection for CE compliance. Click below to find the recommended gloves for handling this product.




Cross-Coupling Guide
Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

Natural Amino Acid Building Blocks for Peptide Synthesis

With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.1 Today, the most common synthetic approaches to medium and even large peptide...
Matthias Junkers
Aldrich ChemFiles 2008, 8.7, 22.
Keywords: Building blocks, Chemfiles, Methods, Peptide synthesis, Peptidomimetics, Solid phase peptide synthesis

Peer-Reviewed Papers
15

References

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