• USA Home
  • 94591 - (S)-Fmoc-3-(trifluoromethyl)-β-Homophe-OH

EMAIL THIS PAGE TO A FRIEND
94591 Sigma-Aldrich

(S)-Fmoc-3-(trifluoromethyl)-β-Homophe-OH

≥97.0% (HPLC)

Synonym: (S)-3-(Fmoc-amino)-4-[3-(trifluoromethyl)phenyl]butyric acid, Fmoc-3-(trifluoromethyl)-L-β-homophenylalanine

Purchase

Properties

Related Categories Beta-Amino Acids, Chemical Biology, Chemical Synthesis, Peptide Synthesis and Peptide Chemistry, Unnatural Amino Acids & Derivatives More...
assay   ≥97.0% (HPLC)
application(s)   peptide synthesis: suitable
functional group   Fmoc
storage temp.   2-8°C
SMILES string   OC(=O)C[C@H](Cc1cccc(c1)C(F)(F)F)NC(=O)OCC2c3ccccc3-c4ccccc24
InChI   1S/C26H22F3NO4/c27-26(28,29)17-7-5-6-16(12-17)13-18(14-24(31)32)30-25(33)34-15-23-21-10-3-1-8-19(21)20-9-2-4-11-22(20)23/h1-12,18,23H,13-15H2,(H,30,33)(H,31,32)/t18-/m0/s1
InChI key   SHSVTUCIAQWRSI-SFHVURJKSA-N

Description

Packaging

500 mg in poly tube

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis (COA)

Please Enter a Lot Number
Protocols & Articles

Articles

β-Amino Acids and Homologs

Although they are less abundant than their α-analogues, β-amino acids occur in nature both in free form and bound to peptides. Oligomers composed exclusively of β-amino acids (so-called β-peptides) m...
Matthias Junkers
Aldrich ChemFiles 2008, 8.7, 11.
Keywords: Chemfiles, Degradations, Metabolism, Peptidomimetics

Related Products

Technical Service:

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Bulk Ordering & Pricing:

Need larger quantities for your development, manufacturing or research applications?