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95471 Aldrich

(−)-Boc-L-thioproline

puriss. p.a., for peptide synthesis, ≥99.0% (HPLC)

Synonym: (−)-(R)-Boc-4-thiazolidinecarboxylic acid, (−)-Boc-L-thiaproline, Boc-4-Thio-Pro-OH, Boc-Thi-OH

  • CAS Number 51077-16-8

  • Empirical Formula (Hill Notation) C9H15NO4S

  • Molecular Weight 233.28

  •  Beilstein Registry Number 4254605

  •  MDL number MFCD00077002

  •  PubChem Substance ID 57653682

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Properties

Related Categories Chemical Biology, Chemical Synthesis, Other Unnatural Amino Acids & Derivatives, Peptide Chemistry, Unnatural Amino Acids & Derivatives More...
grade   for peptide synthesis
InChI Key   FJWNZTPXVSWUKF-LURJTMIESA-N
grade   puriss. p.a.
assay   ≥99.0% (HPLC)
optical activity   [α]20/D −115±3°, c = 1% in methanol

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

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