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47561 Aldrich

Fmoc-Trp(Boc)-OH

≥97.0% (HPLC)

Synonym: Nα-Fmoc-N(in)-Boc-L-tryptophan, N(in)-Boc-Nα-Fmoc-L-tryptophan

  • CAS Number 143824-78-6

  • Empirical Formula (Hill Notation) C31H30N2O6

  • Molecular Weight 526.58

  •  Beilstein Registry Number 7698009

  •  MDL number MFCD00153366

  •  PubChem Substance ID 24871151

  •  eCl@ss 32160406

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Properties

Related Categories Amino Acids & Derivatives, Chemical Biology, Chemical Synthesis, Peptide Chemistry, Standard Fmoc Amino Acids,
InChI Key   ADOHASQZJSJZBT-SANMLTNESA-N
assay   ≥97.0% (HPLC)
optical activity   [α]20/D −21±2°, c = 1% in DMF
storage temp.   2-8°C

Description

Packaging

5, 25 g in poly bottle

Price and Availability

Suggested Laboratory Gloves


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Cross-Coupling Guide
Safety & Documentation

Safety Information

Symbol 
Signal word 
Warning
Hazard statements 
Precautionary statements 
RIDADR 
UN 3077 9 / PGIII
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

Related Content

Indoles, Purines, and Their Isosteres

Substituted indoles and purines have frequently been referred to as “privileged structures” since they are capable of binding to multiple receptors with high affinity, and thus have applications acro...
Keywords: Building blocks, Medicinal chemistry

Peer-Reviewed Papers
15

References

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