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47517 Aldrich

Fmoc-Hyp(tBu)-OH

≥98.0% (HPLC)

Synonym: Fmoc-O-tert-butyl-L-hydroxyproline

  • CAS Number 122996-47-8

  • Empirical Formula (Hill Notation) C24H27NO5

  • Molecular Weight 409.47

  •  Beilstein Registry Number 6161467

  •  MDL number MFCD00151930

  •  PubChem Substance ID 57650984

  •  eCl@ss 32160406

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Properties

Related Categories Chemical Biology, Chemical Synthesis, Peptide Chemistry, Proline Derivatives, Unnatural Amino Acids & Derivatives More...
InChI Key   WPBXBYOKQUEIDW-VFNWGFHPSA-N
assay   ≥98.0% (HPLC)
optical activity   [α]20/D −25±2.5°, c = 1% in methanol
storage temp.   2-8°C

Description

Packaging

5 g in poly bottle

Price and Availability


Laboratory Gloves

Cross-Coupling Guide
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

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

Peer-Reviewed Papers
15

References

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