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14982 Sigma-Aldrich

Boc-β3-Homopro-OH

≥98.0% (TLC)

Synonym: (S)-2-(1-Boc-2-pyrrolidinyl)acetic acid, Boc-L3-homoproline

  • CAS Number 56502-01-3

  • Empirical Formula (Hill Notation) C11H19NO4

  • Molecular Weight 229.27

  •  Beilstein/REAXYS Number 478306

  •  MDL number MFCD01862939

  •  PubChem Substance ID 57647241

  •  NACRES NA.22

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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% (TLC)
SMILES string   CC(C)(C)OC(=O)N1CCC[C@H]1CC(O)=O
InChI   1S/C11H19NO4/c1-11(2,3)16-10(15)12-6-4-5-8(12)7-9(13)14/h8H,4-7H2,1-3H3,(H,13,14)/t8-/m0/s1
InChI key   GDWKIRLZWQQMIE-QMMMGPOBSA-N

Description

Packaging

1 g in poly tube

Other Notes

Building block for necine alkaloids; Synthesis of new analogs of arginine-vasopressin.

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

Peer-Reviewed Papers
15

References

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