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47628 Sigma-Aldrich

Fmoc-Ile-OH

≥98.0% (T)

Synonym: N-(9-Fluorenylmethoxycarbonyl)-L-isoleucine, Fmoc-L-isoleucine

  • CAS Number 71989-23-6

  • Empirical Formula (Hill Notation) C21H23NO4

  • Molecular Weight 353.41

  •  Beilstein/REAXYS Number 4716717

  •  EC Number 276-255-9

  •  MDL number MFCD00037125

  •  eCl@ss 32160406

  •  PubChem Substance ID 57651048

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Properties

Related Categories Amino Acids & Derivatives, Catalysis and Inorganic Chemistry, Chemical Biology, Chemical Synthesis, Isoleucine,
InChI Key   QXVFEIPAZSXRGM-DJJJIMSYSA-N
assay   ≥98.0% (T)
optical activity   [α]20/D −12±1°, c = 1% in DMF
mp   145-147 °C (lit.)
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

50 g in glass bottle

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

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Certificate of Origin

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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

Peer-Reviewed Papers
15

References

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