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670898 Sigma-Aldrich

Fmoc-β-(2-thienyl)-Ala-OH

≥98.0%

Synonym: (S)-2-(Fmoc-amino)-3-(2-thienyl)propionic acid, Fmoc-3-(2-thienyl)-L-alanine

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Properties

Related Categories Alanine Derivatives, Chemical Biology, Chemical Synthesis, Peptide Chemistry | Peptide Synthesis, Unnatural Amino Acids & Derivatives More...
InChI Key   PXBMQFMUHRNKTG-FQEVSTJZSA-N
assay   ≥98.0%

Description

Packaging

1 g in poly tube

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

Protocols & Articles

Articles

Unnatural Amino Acids - ChemFiles 2008, 8.7, 3.

Unnatural amino acids, the non-proteinogenic amino acids that either occur naturally or are chemically synthesized, are becoming more and more important as tools for modern drug discovery research. D...
Matthias Junkers
ChemFiles 2008, 8.7, 3.
Keywords: Absorption, Addition reactions, Alkylations, Asymmetric synthesis, Building blocks, Degradations, Drug discovery, Metabolism, Molecular probes, Peptidomimetics, Pharmaceutical

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