77055-30-2

Usage

Uses

Used in Military and Industrial Applications:
4-tert-Butyl-2,6-dinitroanisole is used as a booster or intermediate explosive for its high sensitivity and performance, making it suitable for various military and industrial uses.
Used in Propellants and Ammunition:
Tetryl is used as a component in propellants and ammunition due to its ability to provide a powerful and reliable explosion, enhancing the effectiveness of these products.
Used in Blasting Agents:
In the mining and construction industries, 4-tert-Butyl-2,6-dinitroanisole is used in blasting agents to facilitate the controlled demolition of structures and the extraction of minerals.
Regulation and Safety:
Due to its hazardous nature, tetryl has been classified as a hazardous material. Its production, handling, and transportation are subject to strict regulations to prevent accidents and minimize environmental impact.

InChI:InChI=1/C11H14N2O5/c1-11(2,3)7-5-8(12(14)15)10(18-4)9(6-7)13(16)17/h5-6H,1-4H3

Upstream product

• 5396-38-3 1-(tert-butyl)-4-methoxybenzene 
• 100-66-3 methoxybenzene 
• 74-88-4 methyl iodide 

Downstream Products

• 33629-47-9 Amchem 70-25 
• 51-28-5 2,4-Dinitrophenol 
• 473269-70-4 5-tert-butyl-2-methoxybenzene-1,3-diamine 
• 1351997-22-2 (5-tert-butyl-3-methanesulfonylamino-2-methoxy-phenyl)-carbamic acid 2,2,2-trichloro-ethyl ester 

Relevant academic research and scientific papers

Novel chromene diarylurea compounds, and preparation method and application thereof

The invention relates to compounds represented by the general formula I, or isomers, pharmaceutical salts and solvates thereof; the invention also relates to a composition containing the compounds represented by the general formula I, or the isomers, the

7-(Piperazine-1-Ymethyl)-1H-Indole-2-Carboxylic Acid (Phenyl)-Amide Derivatives and Allied Compounds as P38 Map Kinase Inhibitors for the Treatment of Respiratory Diseases

The present invention provides compounds according to general formula (I) which are proposed for the treatment of respiratory complaints, particularly asthma and COPD.

1,4-Disubstituted benzo-fused compounds

Disclosed are novel 1,4-disubstituted benzo-fused compounds wherein G, X, L, Q, n and Y are defined herein. The compounds are useful in pharmaceutic compositions for treating diseases or pathological conditions involving inflammation such as chronic infla

Compounds useful as anti-inflammatory agents

Disclosed are novel aromatic compounds of the formula(I) wherein G, E, W, Ar, X, Y and Z. The compounds are useful for treating diseases or pathological conditions involving inflammation such as chronic inflammatory diseases. Also disclosed are pharmaceutical compositions containing and processes of making such compounds.

Novel carbamate and oxamide compounds

Disclosed are novel aromatic compounds of the formula(I) described herein, wherein G, E, W, Ar, X, Y and Z are disclosed herein. The compounds are useful for treating cytokine mediated diseases or conditions such as chronic inflammatory diseases. Also disclosed are pharmaceutical compositions containing and processes of making such compounds.

Compounds useful as anti-inflammatory agents

Disclosed are novel aromatic compounds of the formula(I) wherein G, E, W, Ar, X, Y and Z. The compounds are useful for treating diseases or pathological conditions involving inflammation such as chronic inflammatory diseases. Also disclosed are pharmaceutical compositions containing and processes of making such compounds.

Process for producing N-alkyl-dinitroalkylanilines

This invention relates to a process for producing N-alkyl-dinitroalkylaniline and particularly N-sec-butyl-4-tert-butyl-2,6-dinitroaniline by methylation of an alkylphenol followed by a one or two stage dinitration of the resulting alkylanisole which is followed by reaction with an amine.

THE FORMATION OF 2-ACYLAMINO-4-t-BUTYL-6-NITROPHENOLS BY THE PHOTO-IRRADIATION OF 1-ALKOXY-4-t-BUTYL-2,6-DINITROBENZENES.

The photo-irradiation of 1-methoxy-, 1-ethoxy-, and 1-n-propoxy-4-t-butyl-2,6-dinitrobenzenes gave 2-formylamino-, 2-acetylamino-, and 2-propanoylamino-4-t-butyl-6-nitrophenols, respectively.The structures of these photo-irradiation products were confirme