cas 101-16-6|| where to buy 3-Methoxydiphenylamine

Produktname:3-Methoxydiphenylamine

IUPAC Name:3-methoxy-N-phenylaniline

: CAS：101-16-6; Molekulare Formel：C13H13NO; Reinheit：95%+

: Katalognummer：CM243643; Molekulargewicht：199.25

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CM243643-500g	in stock	ƛǜŵ
CM243643-1000g	in stock	Ȑǜƥ

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Produkt-Details

: CAS-Nr.:101-16-6; Molekulare Formel:C13H13NO; Schmelzpunkt:-; SMILES-Code:COC1=CC(NC2=CC=CC=C2)=CC=C1; Dichte:

: Katalognummer:CM243643; Molekulargewicht:199.25; Siedepunkt:329.8°C at 760 mmHg; Mdl-Nr.:MFCD00008383; Lagerung:Keep in dark place, store at 2-8°C.

Category Infos

: Benzenes; Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

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Product Other Information

Product Overview	3-Methoxydiphenylamine (3-MDA) is a chemical compound that has recently gained attention due to its potential applications in scientific research, particularly in the fields of biochemistry and physiology. This compound is a derivative of diphenylamine and is composed of a nitrogen-containing aromatic ring with a methoxy group attached to one of the ring's carbon atoms. 3-MDA has been used in a variety of studies, and its unique properties make it an interesting tool for research.
Synthesis and Application	3-Methoxydiphenylamine is synthesized using a two-step reaction. The first step involves the reaction of diphenylamine with dimethyl sulfate in the presence of a base, such as sodium hydroxide, to form the corresponding sulfonated diphenylamine. The second step involves the reaction of the sulfonated diphenylamine with methanol in the presence of a base, such as potassium carbonate, to form 3-Methoxydiphenylamine. 3-Methoxydiphenylamine has been used in a variety of studies, including those related to biochemistry and physiology. It has been used as an inhibitor of monoamine oxidase B, an enzyme that plays a role in the metabolism of neurotransmitters. It has also been used as a tool to study the effects of drugs on the nervous system. In addition, 3-Methoxydiphenylamine has been used to study the effects of oxidative stress on cells, as well as to investigate the mechanisms of action of various drugs.
Future Directions	There are a number of potential future directions for research involving 3-Methoxydiphenylamine. For example, further studies could be conducted to better understand the mechanisms of action of 3-Methoxydiphenylamine and to investigate its potential therapeutic applications. In addition, 3-Methoxydiphenylamine could be used to study the effects of drugs on the nervous system and to investigate the potential for using it as an antioxidant. Finally, further research could be conducted to explore the potential of 3-Methoxydiphenylamine as a tool for studying the effects of oxidative stress on cells.