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15544 Aldrich

Boc-Hyp-OH

≥98.0% (TLC)

Synonym: trans-N-(tert-Butoxycarbonyl)-4-hydroxy-L-proline, Boc-L-hydroxyproline

  • CAS Number 13726-69-7

  • Empirical Formula (Hill Notation) C10H17NO5

  • Molecular Weight 231.25

  •  Beilstein Registry Number 4295484

  •  MDL number MFCD00053370

  •  PubChem Substance ID 24849532

  •  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   BENKAPCDIOILGV-RQJHMYQMSA-N
assay   ≥98.0% (TLC)
optical activity   [α]20/D −53.5±2°, c = 1% in DMF
mp   123-127 °C(lit.)

Description

Packaging

5, 25 g in poly bottle

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.




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

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