55776-17-5

Usage

Uses

Used in Pharmaceutical Industry:
2,6-DIMETHOXY-3-NITROBENZOIC ACID is used as an intermediate in the synthesis of various pharmaceuticals for its unique reactivity and functional groups, contributing to the development of new drugs and therapeutic agents.
Used in Organic Chemistry:
2,6-DIMETHOXY-3-NITROBENZOIC ACID is used as a reagent in chemical reactions, facilitating the formation of new compounds and aiding in the advancement of organic chemistry.
Used in Research and Laboratory Settings:
2,6-DIMETHOXY-3-NITROBENZOIC ACID is used as a reference standard for analytical methods, ensuring the accuracy and reliability of experimental results in scientific research.
Used in the Production of Other Substances:
2,6-DIMETHOXY-3-NITROBENZOIC ACID is used as a starting material for the production of other substances, playing a crucial role in the synthesis of a variety of compounds for different applications.

InChI:InChI=1/C9H9NO6/c1-15-6-4-3-5(10(13)14)8(16-2)7(6)9(11)12/h3-4H,1-2H3,(H,11,12)

Downstream Products

• 32541-64-3 2,6-dimethoxy-3-nitrobenzoyl chloride 
• 194291-38-8 (3-Amino-2,6-dimethoxy-phenyl)-phenyl-methanone 
• 194291-32-2 (2,6-Dimethoxy-3-nitro-phenyl)-phenyl-methanone 
• 106567-20-8 2,6-Dimethoxy-N,N-dimethyl-3-nitro-benzamide 
• 106567-32-2 2,6-Dimethoxy-N,N-dimethyl-3-nitro-benzamide 
• 106567-51-5 2,6-Dimethoxy-N,N-dimethyl-3-nitro-benzamide 
• 96897-91-5 N-((S)-1-Ethyl-pyrrolidin-2-ylmethyl)-2-hydroxy-6-methoxy-3-nitro-benzamide 
• 96897-89-1 N-((S)-1-Ethyl-pyrrolidin-2-ylmethyl)-2,6-dimethoxy-3-nitro-benzamide 
• 617244-64-1 N-(2-dimethylamino-ethyl)-2,6-dimethoxy-3-nitro-benzamide 
• 179626-86-9 (2,6-dimethoxy-3-nitrophenyl)methanol 
• 1435943-60-4 2-bromo-1,3-dimethoxy-4-nitrobenzene 
• 1452840-68-4 5'-O-[N-(2,6-dimethoxy-3-nitrobenzoyl)sulfamoyl]cytidine 
• 1000620-02-9 N-[2,6-dimethyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenyl]-3-(4-fluoro-benzoylamino)-2,6-dimethoxy-benzamide 

Relevant academic research and scientific papers

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.