42087-82-1

Usage

Uses

Used in Organic Chemistry:
Methyl 2,6-Dinitrobenzoate is used as a reagent for its high reactivity, which is instrumental in the synthesis and production of various organic compounds. Its role in the formation of aromatic compounds is particularly noteworthy.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, Methyl 2,6-Dinitrobenzoate is utilized as a precursor in the synthesis of various pharmaceuticals. Its contribution to the development of new drugs and chemical products is significant.
Used in Chemical Product Synthesis:
Beyond pharmaceuticals, Methyl 2,6-Dinitrobenzoate is also employed in the synthesis of other chemical products. Its versatility in chemical reactions and its capacity to form a range of compounds make it a valuable asset in the chemical industry.

InChI:InChI=1/C8H6N2O6/c1-16-8(11)7-5(9(12)13)3-2-4-6(7)10(14)15/h2-4H,1H3

Upstream product

• 67-56-1 methanol 
• 59858-28-5 2,6-dinitrobenzoyl chloride 
• 603-12-3 2,6-dinitrobenzoic acid 
• 77-78-1 dimethyl sulfate 
• 20667-76-9 1-methyl-3-(4-methylphenyl)-triazene 
• 606-20-2 2,6-dinitrotoluene 

Downstream Products

• 60472-28-8 Tetramethyl 2,2'-(2-carbomethyloxyphenylene-1,3-diimino)dibutenedioate 
• 32114-64-0 methyl 2,6-diaminobenzoate 
• 53600-33-2 6-methoxyanthranilic acid 
• 54166-96-0 methyl 2-amino-6-methoxybenzoate 
• 77901-52-1 methyl 2-methoxy-6-nitrobenzoate 

Relevant academic research and scientific papers

An Improved Synthesis of 6-Methoxyanthranilic Acid

6-Methoxyanthranilic acid (1) is prepared in three steps from 2,6-dinitrobenzoic acid (6) in an overall yield of 46percent.

Derivatives of 4,6 dioxopyrido[3,2-g]quinoline 2,8 dicarboxylic acid

Novel chemical compounds of the formula: SPC1 Wherein R is selected from the group consisting of hydrogen, alkyl from one to three carbon atoms, inclusive, phenyl, alkali metal, or an amine cation; X and Y can be the same or different and are selected from the group consisting of hydrogen, alkyl of from one to six carbon atoms, inclusive, cycloalkyl of 5 or 6 carbon atoms, inclusive, phenyl, hydroxyl, alkoxy having from one to three carbon atoms, inclusive, halogen, trifluoromethyl, cyano, carboxyamide and O C-OQ, EQU1 where Q is selected from the group consisting of hydrogen, alkyl from one to three carbon atoms, inclusive, alkali metal, and an amine cation, with the proviso that where R is hydrogen, alkali metal or an amine cation, then Q is the same as R, and where R is phenyl or alkyl from one to three carbon atoms, then Q is phenyl or alkyl from one to three carbon atoms; and Z is selected from the group consisting of hydrogen, alkyl from one to three carbon atoms, inclusive, and phenyl. The compounds are formulated with pharmaceutical carriers for oral or parenteral administration, with insufflation being the preferred method. The compositions are useful in the prophylactic treatment of sensitized humans and mammals for allergy and all anaphylactic reactions of a reagin or non-reagin mediated nature.

Cyano phenylene dioxamic molecules

Compounds represented below SPC1 And pharmaceutical compositions thereof, the compositions including the non-substituted phenylene dioxamates are useful in the prophylactic treatment of sensitized mammals for allergy and all anaphylactic reactions of a reagin or non-reagin mediated nature.