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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

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

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