40294-27-7

Usage

Type of compound

Dinitrobenzene derivative

Uses

a. Production of dyes
b. Reagent in organic synthesis

Physical appearance

Yellow to orange crystalline solid

Solubility

Insoluble in water

Ingestion

Toxic

Inhalation

Toxic

Skin contact

Toxic

Health hazards

a. Respiratory system irritation
b. Skin irritation

Safety precautions

Handle with care and follow proper safety procedures when working with it.

Upstream product

• 4992-63-6 4-Nitro-1,2-diethoxybenzene 
• 120-80-9 benzene-1,2-diol 
• 2050-46-6 1,2-diethoxybenzene 

Downstream Products

• 86723-14-0 1,2-diethoxy-4,5-diaminobenzene 

Relevant academic research and scientific papers

Capsule formation in novel cadmium cluster metallocavitands

We report the synthesis and characterization of a new heptanuclear cadmium cluster complex formed within a Schiff base macrocycle and study its surprising dimerization in the solid-state and solution to form capsules. The Royal Society of Chemistry.

Acetoxylation of 6,7-dialkoxy-substituted 1,4-dihydroquinoxaline-2,3-diones (QXs) using fuming nitric acid in acetic acid: A facile synthesis of 5-acyloxy-6,7-dialkoxy QXs

Treatment of 6,7-dialkoxy-1,4-dihydroquinoxaline-2,3-diones 3 with fuming nitric acid in acetic acid at 25°C resulted in an acetoxylation reaction, giving 5-acetoxy-6,7-dialkoxy-1,4-dihydroquinoxaline-2,3-diones 4 in moderate yields. A mechanism involving ipso attack of nitronium ion as the first step is proposed.