Produktname:3-Amino-4-chlorophenol

IUPAC Name:3-amino-4-chlorophenol

CAS:16026-77-0
Molekulare Formel:C6H6ClNO
Reinheit:95%+
Katalognummer:CM249909
Molekulargewicht:143.57

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Produkt-Details

CAS-Nr.:16026-77-0
Molekulare Formel:C6H6ClNO
Schmelzpunkt:-
SMILES-Code:NC1=C(Cl)C=CC(O)=C1
Dichte:
Katalognummer:CM249909
Molekulargewicht:143.57
Siedepunkt:282.8°C at 760 mmHg
Mdl-Nr.:MFCD03427127
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.

Column Infos

Product Other Information

Product Overview 3-Amino-4-chlorophenol (3-APC) is a widely used chemical compound found in pharmaceuticals, cosmetics, and many other products. It is a derivative of phenol and is used in a variety of applications due to its unique properties. It is an important intermediate in the synthesis of many compounds, including drugs and pesticides. 3-APC has a wide range of applications, including as a preservative, antiseptic, and disinfectant. It also has potential applications in the medical field, such as in the treatment of cancer and other diseases.
Synthesis and Application 3-Amino-4-chlorophenol is typically synthesized through a process known as the Friedel-Crafts acylation reaction. This reaction involves the reaction of an acyl chloride with an aromatic compound in the presence of a Lewis acid catalyst. The reaction produces an acylated product, which is then treated with a base to form the desired product. The reaction is typically conducted at a temperature of 80-90°C in an inert atmosphere. 3-Amino-4-chlorophenol has been studied extensively in scientific research due to its wide range of applications. It has been used as a model compound to study the interactions between proteins and small molecules, as well as its effects on cell growth and metabolism. It has also been studied as a potential therapeutic agent in the treatment of cancer, Alzheimer’s disease, and other diseases. Additionally, 3-Amino-4-chlorophenol has been used as a model compound to study the effects of environmental pollutants on the environment.
Future Directions The potential applications of 3-Amino-4-chlorophenol are vast and there are many future directions that can be explored. One potential direction is to further investigate the use of 3-Amino-4-chlorophenol as a therapeutic agent in the treatment of cancer and other diseases. Additionally, further research could be conducted to explore the use of 3-Amino-4-chlorophenol as a preservative, antiseptic, and disinfectant. Furthermore, further research could be conducted to study the effects of 3-Amino-4-chlorophenol on the environment and its potential applications in the medical field. Finally, further research could be conducted to explore the potential of 3-Amino-4-chlorophenol as an inhibitor of certain enzymes, proteins, and drugs.