Substance
ID:321723
Names and Identifiers
IUPAC Traditional name
1-[(9H-fluoren-9-ylmethoxy)carbonyl]piperidine-2-carboxylic acid
IUPAC name
1-[(9H-fluoren-9-ylmethoxy)carbonyl]piperidine-2-carboxylic acid
Synonyms
Fmoc-DL-哌啶甲酸N-Fmoc-piperidine-2-carboxylic acid1,2-Piperidinedicarboxylic acid, 1-(9H-fluoren-9-ylmethyl) esterFmoc-DL-pipecolic acidN-Fmoc-哌啶-2-甲酸
Properties
Safety Information
UN Number
3077
MSDS Link
Safety Statements
60-61
Storage Temperature
2-8°C
RID/ADR
UN 3077 9/PG 3
Risk Statements
50/53
GHS Pictograms
Hazardous to the aquatic environment
Acute hazard, category1
Chronic hazard, categories 1,2
European Hazard Symbols
Nature polluting (N)Packing Group
3
German water hazard class
3
GHS Signal Word
Warning
GHS Hazard statements
H400
GHS Precautionary statements
P273
Hazard Class
9
Product Information
Purity
97%
Empirical Formula (Hill Notation)
C21H21NO4
Physical Property
Melting Point
113-120 °C
Molecule Details
Packaging
1, 5 g in glass bottle
Application
Reactant for racemic solid-phase preparation of human protease activated receptor 2 agonists and antagonists1Analyte for urea-linked cinchona-calexarene hybrid type receptors for chromatographic enantiomer separation of carbamate-protected amino acids2Combinatorial reactant for assembly of alkylglycine library arrays by SPOT technique on cellulose membranes for identification of micromolar ligands for monoclonal antibodies3
1, 5 g in glass bottle
Application
Reactant for racemic solid-phase preparation of human protease activated receptor 2 agonists and antagonists1Analyte for urea-linked cinchona-calexarene hybrid type receptors for chromatographic enantiomer separation of carbamate-protected amino acids2Combinatorial reactant for assembly of alkylglycine library arrays by SPOT technique on cellulose membranes for identification of micromolar ligands for monoclonal antibodies3
Molecular Spectra
No Data Available
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References
No Data Available
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