Produktname:2-(N-Boc-N-methylamino)ethylamine

IUPAC Name:tert-butyl N-(2-aminoethyl)-N-methylcarbamate

CAS:121492-06-6
Molekulare Formel:C8H18N2O2
Reinheit:95%
Katalognummer:CM117467
Molekulargewicht:174.24

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Produkt-Details

CAS-Nr.:121492-06-6
Molekulare Formel:C8H18N2O2
Schmelzpunkt:-
SMILES-Code:NCCN(C(OC(C)(C)C)=O)C
Dichte:
Katalognummer:CM117467
Molekulargewicht:174.24
Siedepunkt:
Mdl-Nr.:MFCD01317789
Lagerung:

Column Infos

Nitrogen Compounds
Nitrogen compounds can be classified as mineral or organic. Mineral compounds are essentially formed by the ammonium ion (NH4+), which is generated when ammonium salts are dissolved in water. Organic compounds, in contrast, are carbon and hydrogen compounds that contain a nitrogen atom. All organic nitrogen-containing compounds can be considered as derivatives of ammonia in which one or more hydrogen atoms are substituted by hydrocarbon radicals.

Product Other Information

Product Overview N-Boc-N-methylethylenediamine (Boc-MEDA) is a bifunctional amine that can be used as a ligand, protecting group, and as a reagent in organic synthesis. 
Synthesis Method N-Boc-N-methylethylenediamine is synthesized through the reaction of N-Boc-N-methyl-2-aminopyridine with ethylenediamine. This reaction is typically carried out in aqueous solution at room temperature and is often catalyzed by a base, such as sodium hydroxide.
Chemical Properties It is relatively easy to synthesize, is readily available, and is relatively inexpensive. It can be toxic if not handled properly.
Synthesis and Application It can be used as a ligand in coordination chemistry, as a protecting group in organic synthesis, and as a reagent in organic synthesis. N-Boc-N-methylethylenediamine is also used in drug delivery, catalysis, and imaging. Additionally, N-Boc-N-methylethylenediamine is used in the synthesis of a variety of compounds, including peptides and peptidomimetics.
Future Directions The use of N-Boc-N-methylethylenediamine as a reagent in peptide synthesis, as a stabilizer in drug delivery, and as a catalyst in catalysis. Additionally, future research could focus on the development of new methods for the synthesis of N-Boc-N-methylethylenediamine, as well as the development of new methods for the use of N-Boc-N-methylethylenediamine in laboratory experiments. Furthermore, future research could focus on the development of new methods for the detection and quantification of N-Boc-N-methylethylenediamine in biological samples. Finally, future research could focus on the development of new methods for the delivery of N-Boc-N-methylethylenediamine to specific areas of the body.