51652-35-8

Usage

Uses

Used in Dye Manufacturing:
5-METHOXY-2,4-DINITROPHENOL is used as a key intermediate in the production of various dyes, contributing to the development of colorants for different applications.
Used in Explosive Production:
Due to its high explosive properties, 5-METHOXY-2,4-DINITROPHENOL is used as a component in the manufacturing of explosives, providing a reactive substance for blasting and demolition purposes.
However, it is important to note that the use of 5-METHOXY-2,4-DINITROPHENOL in these industries must be strictly regulated and controlled to minimize its potential hazards to human health and the environment.

InChI:InChI=1/C7H6N2O6/c1-15-7-3-6(10)4(8(11)12)2-5(7)9(13)14/h2-3,10H,1H3

Upstream product

• 67-56-1 methanol 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 150-19-6 O-methylresorcine 
• 7697-37-2 nitric acid 
• 704-14-3 3-methoxy-6-nitro-phenol 
• 860725-05-9 3,5-dimethoxy-2,6-dinitro-benzaldehyde 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 7732-18-5 water 
• 10365-98-7 3-methoxyphenylboronic acid 
• 3698-83-7 2,4-dichloro-1,5-dinitrobenzene 
• 20278-59-5 4,5-dinitro-2-methoxyaniline 
• 6627-53-8 1-chloro-3-methoxy-4-nitrobenzene 
• 1210-96-4 1,3-dimethoxy-4,6-dinitrobenzene 
• 57356-27-1 5-chloro-2,4-dinitroanisole 

Downstream Products

• 1210-96-4 1,3-dimethoxy-4,6-dinitrobenzene 
• 616-74-0 4,6-dinitroresorcinol 
• 16523-31-2 4,6-diaminoresorcin dihydrochloride 

Relevant academic research and scientific papers

Visible-Light-Induced Radical Polynitration of Arylboronic Acids: Synthesis of Polynitrophenols

We report a visible light-assisted one-pot method for the synthesis of polynitrophenols through radical tandem hydroxylation and nitration of arylboronic acids by utilizing copper(II) nitrate tri-nitydrate as the nitro source. This method features mild conditions, a simple procedure, and good functional group tolerance. Compared to conventional methods, this work provides a straightforward approach for the polynitration of aromatic compounds.

The nitration of electron-rich aromatics

The successful mononitration of a variety of electron-rich aromatic substrates is reported, employing either nitronium tetrafluoroborate or 'claycop' as the nitrating agent. Dinitration of four of the substrates was achieved when employing nitronium tetrafluoroborate. Several of the products have previously been prepared only by indirect methods.

Process for the preparation of diaminoresorcinol

A method of producing 4,6-diaminoresorcinol comprising a) reducing a dinitroarylether of the formula: STR1 wherein R is hydrogen, C1 -C6 alkyl, cycloalkyl or CH=CH2, R' is hydrogen or CH2 --R, each A is independ

Preparation of nitrophenols

A process for the preparation of nitrophenols by adding over a period of time a suspension containing from about 4 to about 20 per cent weight/volume of nitrosated phenol to a nitric acid solution containing between 45 and 100 per cent by weight of nitric acid, said solution being maintained at a temperature in the range from about 45° to 100°C.