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47622 Sigma-Aldrich

Fmoc-Thr(tBu)-OH

≥98.0% (HPLC)

Synonym: Fmoc-O-tert-butyl-L-threonine

  • CAS Number 71989-35-0

  • Empirical Formula (Hill Notation) C23H27NO5

  • Molecular Weight 397.46

  •  Beilstein/REAXYS Number 4581133

  •  EC Number 276-261-1

  •  MDL number MFCD00077075

  •  eCl@ss 32160406

  •  PubChem Substance ID 57651042

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Properties

Related Categories Amino Acids & Derivatives, Catalysis and Inorganic Chemistry, Chemical Biology, Chemical Synthesis, Peptide Synthesis and Peptide Chemistry,
InChI Key   LZOLWEQBVPVDPR-VLIAUNLRSA-N
assay   ≥98.0% (HPLC)
optical activity   [α]20/D +16±1°, c = 1% in ethyl acetate
functional group   amine
  carboxylic acid
reaction suitability   reaction type: C-H Activation
  reagent type: ligand
reaction type: Peptide Synthesis
storage temp.   2-8°C

Description

Packaging

1, 10 g in glass 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

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
ChemFiles 2008, 8.7, 22.
Keywords: Building blocks, Peptide synthesis, Peptidomimetics, Solid phase peptide synthesis

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