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73418 Sigma-Aldrich

Fmoc-D-Pip-OH

≥98.0%

Synonym: (R)-N-Fmoc-piperidine-2-carboxylic acid, N-Fmoc-D-pipecolic acid

  • CAS Number 101555-63-9

  • Empirical Formula (Hill Notation) C21H21NO4

  • Molecular Weight 351.40

  •  Beilstein/REAXYS Number 5485101

  •  MDL number MFCD00235899

  •  PubChem Substance ID 57652477

  •  NACRES NA.26

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Properties

Related Categories Chemical Biology, Chemical Synthesis, Peptide Synthesis and Peptide Chemistry, Proline Derivatives, Unnatural Amino Acids & Derivatives More...
assay   ≥98.0%
storage temp.   2-8°C
SMILES string   OC(=O)[C@H]1CCCCN1C(=O)OCC2c3ccccc3-c4ccccc24
InChI   1S/C21H21NO4/c23-20(24)19-11-5-6-12-22(19)21(25)26-13-18-16-9-3-1-7-14(16)15-8-2-4-10-17(15)18/h1-4,7-10,18-19H,5-6,11-13H2,(H,23,24)/t19-/m1/s1
InChI key   CKLAZLINARHOTG-LJQANCHMSA-N

Description

Packaging

1 g in poly tube

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
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

Proline Derivatives

Proline is a non-polar, natural amino acid that forms a tertiary amide when incorporated into peptides. Thus, it is the only proteinogenic amino acid that does not act as a hydrogen bond donor in a p...
Matthias Junkers
Aldrich ChemFiles 2008, 8.7, 8.
Keywords: Asymmetric synthesis, Chemfiles, Pharmaceutical

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