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338338 Aldrich

Fmoc-Phe-OH

98%

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

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Properties

Related Categories Amino Acid Derivatives, Catalysis and Inorganic Chemistry, Chemical Biology, Chemical Synthesis, Peptide Chemistry,
assay   98%
optical activity   [α]20/D −37°, c = 1 in DMF
mp   180-187 °C(lit.)
storage temp.   2-8°C

Description

Packaging

5, 25 g in glass bottle

Price and Availability

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Safety & Documentation

Safety Information

WGK Germany 
3

Documents

Certificate of Analysis

Certificate of Origin

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

References

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Design and synthesis of new N-(fluorenyl-9-methoxycarbonyl) (Fmoc)-dipeptides as anti-inflammatory agents. Chiao-Ting Yen et al Eur. J. Med. Chem. 44, 1933-40, (2009)

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FT-IR 1 (1), 165:A / FT-NMR 1 (2), 1429:A / RegBook 1 (2), 2051:J / Structure Index 1, 326:D:3

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