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73418 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 Registry Number 5485101

  •  MDL number MFCD00235899

  •  PubChem Substance ID 24886552

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Properties

Related Categories Chemical Biology, Chemical Synthesis, Peptide Chemistry, Proline Derivatives, Unnatural Amino Acids & Derivatives More...
InChI Key   CKLAZLINARHOTG-LJQANCHMSA-N
assay   ≥98.0%
storage temp.   2-8°C

Description

Packaging

1 g in poly tube

Price and Availability

Suggested Laboratory Gloves


Laboratory GlovesThis substance has been tested against several types of hand protection for CE compliance. Click below to find the recommended gloves for handling this product.



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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