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70238 Sigma-Aldrich

1-Fmoc-(S)-azetidine-2-carboxylic acid

≥97.0%

Synonym: 1-Fmoc-L-azetidine-2-carboxylic acid

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Properties

Related Categories Chemical Biology, Chemical Synthesis, Other Unnatural Amino Acids & Derivatives, Peptide Synthesis and Peptide Chemistry, Unnatural Amino Acids & Derivatives More...
assay   ≥97.0%
SMILES string   OC(=O)[C@@H]1CCN1C(=O)OCC2c3ccccc3-c4ccccc24
InChI   1S/C19H17NO4/c21-18(22)17-9-10-20(17)19(23)24-11-16-14-7-3-1-5-12(14)13-6-2-4-8-15(13)16/h1-8,16-17H,9-11H2,(H,21,22)/t17-/m0/s1
InChI key   BXRZCDISGRVJCA-KRWDZBQOSA-N

Description

Packaging

500 mg in poly tube

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

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