cas 69154-03-6|| where to buy 3-Aminohomopiperidine

Produktname:3-Aminohomopiperidine

IUPAC Name:azepan-3-amine

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CM179249-5g	in stock	ĽŢƄ

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: CAS-Nr.:69154-03-6; Molekulare Formel:C6H14N2; Schmelzpunkt:-; SMILES-Code:NC1CCCCNC1; Dichte:

: Katalognummer:CM179249; Molekulargewicht:114.19; Siedepunkt:180.9°C at 760 mmHg; Mdl-Nr.:MFCD02183579; Lagerung:Keep in dark place, store at 2-8°C.

: Azepanes; The use of azepane as a scaffold for drug discovery remains of interest. The azepane linker is the key to efficient activity. A number of seven-membered ring derivatives have been prepared or investigated for their potential or actual pharmacological properties. Examples include azaalkane derivatives as PKB (protein kinase B) inhibitors.

Product Overview	Azepan-3-amine, also known as 3-azabicyclo[3.1.0]hexane, is an organic compound consisting of a six-membered ring with three nitrogen atoms and one carbon atom. It is an aromatic amine and is used in a variety of applications.
Synthesis Method	Azepan-3-amine can be synthesized through a variety of methods, including the cyclization of N-alkyl-2-azetidinones, the condensation of 1,2-diamines and 1,3-diketones, and the reaction of aryl halides with trimethylamine.
Synthesis and Application	The main advantage of using azepan-3-amine in lab experiments is its ease of synthesis. It can be synthesized in high yields with relatively simple reactions. It has been used as a building block for organic synthesis and as a ligand in coordination chemistry. It is also used in the synthesis of drugs, such as the anti-depressant mirtazapine. Additionally, it is used in the synthesis of molecular probes for imaging applications.
Storage and Handling	It is relatively stable and can be stored for long periods of time. The main limitation of using azepan-3-amine in lab experiments is its toxicity. It is toxic if ingested or inhaled, and should be handled with care.