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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

  • CAS Number 130309-35-2

  • Empirical Formula (Hill Notation) C22H19NO4S

  • Molecular Weight 393.46

  •  MDL number MFCD00065676

  •  PubChem Substance ID 329760394

  •  NACRES NA.26

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Properties

Related Categories Alanine Derivatives, Chemical Biology, Chemical Synthesis, Peptide Synthesis and Peptide Chemistry, Unnatural Amino Acids & Derivatives More...
Quality Level   100
assay   ≥98.0%
application(s)   peptide synthesis: suitable
functional group   Fmoc
SMILES string   OC(=O)[C@H](Cc1cccs1)NC(=O)OCC2c3ccccc3-c4ccccc24
InChI   1S/C22H19NO4S/c24-21(25)20(12-14-6-5-11-28-14)23-22(26)27-13-19-17-9-3-1-7-15(17)16-8-2-4-10-18(16)19/h1-11,19-20H,12-13H2,(H,23,26)(H,24,25)/t20-/m0/s1
InChI key   PXBMQFMUHRNKTG-FQEVSTJZSA-N

Description

Packaging

1 g in poly tube

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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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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