55775-99-0

Usage

Molecular weight

256.03 g/mol

Appearance

Yellow crystalline solid

Melting point

88-91°C

Solubility

Slightly soluble in water, soluble in organic solvents like ethanol, acetone, and dichloromethane

Functional groups

Ester, nitro, and chloro groups are present in the molecule.

Reactivity

2,6-Dichloro-3-nitrobenzoic acid methyl ester can undergo various chemical reactions, such as ester hydrolysis, nucleophilic substitution, and electrophilic substitution.

Uses

It is commonly used in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and other organic compounds. It is also a valuable intermediate in the development of new compounds with potential applications in a wide range of industries.

Upstream product

• 55775-97-8 2,6-dichloro-3-nitrobenzoic acid 
• 74-88-4 methyl iodide 
• 50-30-6 2,6-dichlorobenzoic acid 
• 67-56-1 methanol 

Downstream Products

• 635317-47-4 methyl 2,3-diamino-6-chlorobenzoate 
• 635317-46-3 methyl 2-amino-6-chloro-3-nitrobenzoate 
• 851659-04-6 methyl 6-chloro-2-((4-methoxybenzyl)amino)-3-nitrobenzoate 
• 96853-23-5 methyl 6-chloro-2-(methylamino)-3-nitrobenzoate 

Relevant academic research and scientific papers

INHIBITORS OF ALPHA 2 BETA 1 INTEGRIN AND METHODS OF USE THEREOF

Disclosed herein, inter alia, are inhibitors of alpha 2 beta 1 integrin and methods of using the same.

Synthesis method of anti-cancer drug intermediate methyl 2-fluoro-3-aminobenzoate

The invention discloses a synthetic method of 2-fluoro-3-methyl aminobenzoate, and belongs to the technical field of synthesis of medical intermediates. According to the method, 2, 6-dichlorobenzoic acid is taken as a raw material, 2, 6-dichloro-3-nitrobe

COMPOUNDS, COMPOSITIONS AND METHODS OF USE

Herein, compounds, compositions and methods for modulating inclusion formation and stress granules in cells related to the onset of neurodegenerative diseases, musculoskeletal diseases, cancer, ophthalmological diseases, and viral infections are described.

Use of 2,6-Dichlorobenzonitrile (Dichlobenil) as Starting Material for Synthesis of Herbicides, Derivatives of Benzoic Acid.

Results of an investigation are presented in which S//N reactions of dichlobenil and its transformation products were investigated using as nucleophilic agents for chlorine exchange: sodium methanolate and ethanolate, as well as aniline and its derivatives. It has been shown that the ability to enter the reaction of mono- or disubstitution is dependent on the kind of derivative of 2,6-dichloro-3-nitrobenzoic acid, as well as on conditions of reactions. In the manner described above, dichlobenil has been transformed into valuable herbicide, dicamba, i. e. 3,6-dichloro-2-methoxybenzoic acid. A mixture of isomeric acids has been obtained, their herbicide activity having the same range.