Produktname:tert-butyl N-[(1-aminocyclopentyl)methyl]carbamate

IUPAC Name:tert-butyl N-[(1-aminocyclopentyl)methyl]carbamate

CAS:1311318-21-4
Molekulare Formel:C11H22N2O2
Reinheit:97%
Katalognummer:CM106451
Molekulargewicht:214.31

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Produkt-Details

CAS-Nr.:1311318-21-4
Molekulare Formel:C11H22N2O2
Schmelzpunkt:-
SMILES-Code:O=C(OC(C)(C)C)NCC1(N)CCCC1
Dichte:
Katalognummer:CM106451
Molekulargewicht:214.31
Siedepunkt:
Mdl-Nr.:MFCD18483181
Lagerung:

Category Infos

Cyclopentanes
Cyclopentane is a cycloalkane, an organic compound with a molecular formula of C5H10, a colorless and transparent liquid, insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, carbon tetrachloride, acetone, etc. It is mainly used as a solvent and chromatographic reference materials.
Cyclopentanes,where to buy Cyclopentanes
Cyclopentanes
Cyclopentane (also called C pentane) is a highly flammable alicyclic hydrocarbon with chemical formula C5H10 and CAS number 287-92-3, consisting of a ring of five carbon atoms each bonded with two hydrogen atoms above and below the plane. It occurs as a colorless liquid with a petrol-like odor.

Column Infos

Cyclanes
Cyclanes are secondary metabolites that can be found in plants, and are also biochemicals that can be used in medicine. Cyclanes are found in pine trees, and are used in the making of plastics. Cyclenes are found in cinnamon, and have antifungal properties.

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Product Other Information

Product Overview tert-butyl N-[(1-aminocyclopentyl)methyl]carbamate, also known as TBCMC, is a chemical compound used in a variety of scientific research applications. TBCMC has been used in research applications such as synthesis, mechanism of action studies, biochemical and physiological effects, and laboratory experiments.
Synthesis and Application tert-butyl N-[(1-aminocyclopentyl)methyl]carbamate can be synthesized using a variety of methods. The most common method involves the reaction of tert-butyl chloride with N-(1-aminocyclopentyl)methyl carbamate in an aprotic solvent such as dichloromethane. The reaction yields a tert-butyl N-[(1-aminocyclopentyl)methyl]carbamate product. Other methods of synthesis include the reaction of tert-butyl bromide with N-(1-aminocyclopentyl)methyl carbamate in an aprotic solvent such as dichloromethane and the reaction of tert-butyl iodide with N-(1-aminocyclopentyl)methyl carbamate in an aprotic solvent such as dichloromethane. Tert-butyl N-[(1-aminocyclopentyl)methyl]carbamate has been used in a variety of scientific research applications. It has been used as a reagent for the synthesis of other compounds, as a model compound for studying the mechanism of action of drugs, and as an inhibitor of enzyme activity. It has also been used in biochemical and physiological studies to investigate the effects of various compounds on the body. Additionally, it has been used in laboratory experiments to assess the efficacy of various compounds.
Future Directions There are several potential future directions for research with tert-butyl N-[(1-aminocyclopentyl)methyl]carbamate. One area of research is to investigate the effects of tert-butyl N-[(1-aminocyclopentyl)methyl]carbamate on the activity of other enzymes. Additionally, further research could be done to explore the mechanism of action of tert-butyl N-[(1-aminocyclopentyl)methyl]carbamate and to investigate its potential therapeutic effects. Finally, further studies could be done to assess the efficacy of tert-butyl N-[(1-aminocyclopentyl)methyl]carbamate in laboratory experiments.