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11558 Aldrich

Lithium L-aziridine-2-carboxylate

≥97.0% (dried material, NT)

Synonym: L-Aziridine-2-carboxylic acid lithium salt

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Properties

Related Categories Asymmetric Synthesis, Aziridines, Chemical Biology, Chemical Synthesis, Chiral Building Blocks,
InChI Key   ZGQWDLXRNCMIHH-DKWTVANSSA-M
assay   ≥97.0% (dried material, NT)
optical activity   [α]20/D −42±2°, c = 1% in H2O
impurities   ~3% water

Description

Other Notes

Chiral building block; protected derivatives are used for the synthesis of various amino acids by ring-opening with nucleophiles

Packaging

50 mg in glass bottle

Bottomless glass bottle. Contents are inside inserted fused cone.

Application

Lithium L-aziridine-2-carboxylate may be used as a chelate ligand to form complexes with transition metal salts.

Price and Availability

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

Peer-Reviewed Papers
15

References

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