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47912 Sigma-Aldrich

Fmoc-L3-homoproline

≥98.0% (HPLC)

Synonym: (S)-2-(1-Fmoc-2-pyrrolidinyl)acetic acid

  • CAS Number 193693-60-6

  • Empirical Formula (Hill Notation) C21H21NO4

  • Molecular Weight 351.40

  •  Beilstein/REAXYS Number 7798553

  •  MDL number MFCD01863058

  •  PubChem Substance ID 57651136

  •  NACRES NA.26

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Properties

Related Categories Beta-Amino Acids, Chemical Biology, Chemical Synthesis, Peptide Synthesis and Peptide Chemistry, Unnatural Amino Acids & Derivatives More...
assay   ≥98.0% (HPLC)
storage temp.   2-8°C
SMILES string   OC(=O)C[C@@H]1CCCN1C(=O)OCC2c3ccccc3-c4ccccc24
InChI   1S/C21H21NO4/c23-20(24)12-14-6-5-11-22(14)21(25)26-13-19-17-9-3-1-7-15(17)16-8-2-4-10-18(16)19/h1-4,7-10,14,19H,5-6,11-13H2,(H,23,24)/t14-/m0/s1
InChI key   ZNIGOUDZWCDFFC-AWEZNQCLSA-N

Description

Packaging

1 g in poly bottle

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

Proline Derivatives and Analogs

Proline is a non-polar proteinogenic amino acid that forms a tertiary amide when incorporated into peptides. It does not have a hydrogen on the amide group and therefore cannot act as a hydrogen bond...
Chemfiles Volume 5 Article 12
Keywords: Adhesion, Biochemistry, Catalysis, Deposition, Hydroxylations, Isomerizations, Nucleic acid hybridization, Pharmaceutical, Reductions, Substitutions, Type

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

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