Product Name:2,6-dichloro-4-hydroxybenzoic acid

IUPAC Name:2,6-dichloro-4-hydroxybenzoic acid

CAS:4641-38-7
Molecular Formula:C7H4Cl2O3
Purity:95%
Catalog Number:CM125361
Molecular Weight:207.01

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CM125361-1g 3-4 Weeks ƏƏƏ

For R&D use only.

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Product Details

CAS NO:4641-38-7
Molecular Formula:C7H4Cl2O3
Melting Point:-
Smiles Code:O=C(O)C1=C(Cl)C=C(O)C=C1Cl
Density:
Catalog Number:CM125361
Molecular Weight:207.01
Boiling Point:362.6±42.0°C at 760 mmHg
MDL No:
Storage: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 2,6-dichloro-4-hydroxybenzoic acid (2,6-DCBH) is an organic compound that belongs to the family of benzoic acids. It is a white crystalline powder that is soluble in water and organic solvents. The chemical formula of 2,6-DCBH is C7H4Cl2O3, and its molecular weight is 207.01 g/mol. This compound has attracted significant attention in scientific research due to its potential applications in various fields, including medicine, agriculture, and industry.
Synthesis and Application The synthesis of 2,6-dichloro-4-hydroxybenzoic acid can be achieved through several methods, including the reaction of 2,6-dichlorohydroquinone with sodium hydroxide, the oxidation of 2,6-dichlorophenol, and the reaction of 2,6-dichlorophenol with sodium carbonate. The most commonly used method for synthesizing 2,6-dichloro-4-hydroxybenzoic acid is the reaction of 2,6-dichlorohydroquinone with sodium hydroxide. 2,6-dichloro-4-hydroxybenzoic acid has been extensively studied for its potential applications in various scientific research fields. In medicine, it has been shown to have anti-inflammatory and antioxidant properties, making it a potential candidate for the treatment of various diseases, including cancer, diabetes, and cardiovascular diseases. In agriculture, 2,6-dichloro-4-hydroxybenzoic acid has been used as a herbicide due to its ability to inhibit the growth of weeds. In industry, it has been used as a raw material for the production of various chemicals, including dyes and pharmaceuticals.
Future Directions There are several future directions for the research and development of 2,6-dichloro-4-hydroxybenzoic acid. One potential direction is to explore its potential as a treatment for neurodegenerative diseases, such as Alzheimer's and Parkinson's disease. Another direction is to investigate its potential as a natural antioxidant and anti-inflammatory agent in the food industry. Additionally, further research is needed to understand its mechanism of action and potential side effects in humans.