EMAIL THIS PAGE TO A FRIEND
09794 Sigma-Aldrich

Boc-β-Phe-OH

≥96.0% (HPLC)

Synonym: (R)-3-(Boc-amino)-3-phenylpropionic acid, Boc-L-β-phenylalanine

  • CAS Number 161024-80-2

  • Empirical Formula (Hill Notation) C14H19NO4

  • Molecular Weight 265.30

  •  Beilstein/REAXYS Number 5404389

  •  MDL number MFCD01320859

  •  PubChem Substance ID 329748832

  •  NACRES NA.26

Purchase

Properties

Related Categories A - H, Amino Acids, Beta-Amino Acids, Biochemicals and Reagents, Chemical Biology,
Quality Level   100
assay   ≥96.0% (HPLC)
SMILES string   CC(C)(C)OC(=O)N[C@H](CC(O)=O)c1ccccc1
InChI   1S/C14H19NO4/c1-14(2,3)19-13(18)15-11(9-12(16)17)10-7-5-4-6-8-10/h4-8,11H,9H2,1-3H3,(H,15,18)(H,16,17)/t11-/m1/s1
InChI key   JTNQFJPZRTURSI-LLVKDONJSA-N

Description

Application

Boc-L-β-Phenylalanine is an N-terminal protected amino acid used in solid-phase peptide synthesis (SPPS) to make peptides containing β-phenylalanine residues.

Biochem/physiol Actions

Boc-L-β-phenylalanine may be useful in the synthesis of anti-microbial β-peptides.

Safety & Documentation

Safety Information

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

Peer-Reviewed Papers
15

References

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?