cas 61123-70-4|| where to buy 3-(2,3-Dihydro-indol-1-yl)-propylamine

Produktname:3-(2,3-Dihydro-indol-1-yl)-propylamine

IUPAC Name:3-(2,3-dihydro-1H-indol-1-yl)propan-1-amine

Packungseinheit	Verfügbarer Vorrat	Preis($)
CM146635-250mg	in stock	ſȦ
CM146635-1g	in stock	ƻſȷ

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: CAS-Nr.:61123-70-4; Molekulare Formel:C11H16N2; Schmelzpunkt:-; SMILES-Code:NCCCN1CCC2=C1C=CC=C2; Dichte:

: Katalognummer:CM146635; Molekulargewicht:176.26; Siedepunkt:; Mdl-Nr.:MFCD03011732; Lagerung:Store at 2-8°C.

: Indolines; Indoline is an aromatic heterocyclic organic compound with the chemical formula C8H9N. The compound is based on the indole structure, but the 2-3 bond is saturated. Indoles and their derivatives continue to inspire the development of synthetic organic chemistry even years after their discovery. The specific scaffold is a privileged structure and is ubiquitous in pharmaceuticals and biologically active compounds. Fused indolines as indole derivatives are of particular interest as they are often found in natural products and bioactives such as strychnine and tryptanthrins (alkaloids), mitosanes and mitosenes (antitumor activity) and isatisine (antiviral activity).

Product Overview	3-(2,3-Dihydro-indol-1-yl)-propylamine (61123-70-4), is an endogenous compound found in mammalian tissues and is widely studied for its potential role in the regulation of metabolism and inflammation. It is a derivative of tryptophan, an essential amino acid, and is synthesized by the enzyme tryptophan hydroxylase. 3-(2,3-Dihydro-indol-1-yl)-propylamine has been found to be involved in numerous physiological processes, including the regulation of glucose and lipid metabolism, and inflammation.
Physical Properties	3-(2,3-Dihydro-indol-1-yl)-propylamine is a yellow oil.
Chemical Properties	3-(2,3-Dihydro-indol-1-yl)-propylamine is a reactive compound, often utilized as a starting material or intermediate in various chemical reactions and synthesis processes.
Synthesis and Application	3-(2,3-Dihydro-indol-1-yl)-propylamine has been studied extensively in recent years due to its potential role in the regulation of metabolism and inflammation. It has been found to be involved in numerous physiological processes, including the regulation of glucose and lipid metabolism, and inflammation. In addition, 3-(2,3-Dihydro-indol-1-yl)-propylamine has been studied for its potential role in the regulation of neuronal excitability, and its involvement in the pathogenesis of neurodegenerative diseases such as Alzheimer’s and Parkinson’s.
Storage and Handling	Store 3-(2,3-Dihydro-indol-1-yl)-propylamine at 2-8°C and protect it from light.