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47633 Aldrich

Fmoc-Leu-OH

≥97.0%

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

  • CAS Number 35661-60-0

  • Empirical Formula (Hill Notation) C21H23NO4

  • Molecular Weight 353.41

  •  Beilstein Registry Number 2178254

  •  EC Number 252-662-7

  •  MDL number MFCD00037133

  •  PubChem Substance ID 57651051

  •  eCl@ss 32160406

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Properties

Related Categories Amino Acids & Derivatives, Catalysis and Inorganic Chemistry, Chemical Biology, Chemical Synthesis, Leucine,
InChI Key   CBPJQFCAFFNICX-IBGZPJMESA-N
assay   ≥97.0%
optical activity   [α]20/D −25±2°, c = 1% in DMF
mp   152-156 °C(lit.)
  152-156 °C
storage temp.   2-8°C

Description

Biochem/physiol Actions

PPARγ ligand that induces insulin sensitization, but not adipogenesis.

Packaging

5, 50 g in glass bottle

Price and Availability


Cross-Coupling Guide
Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

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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