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Usage

Uses

Used in Chemical Synthesis:
2,4,6-Trinitrobenzoyl chloride is used as a chemical intermediate for the synthesis of various organic compounds, such as dyes, pharmaceuticals, and pesticides. Its reactivity allows for the creation of a wide range of products with diverse applications across different industries.
Used in Explosive and Propellant Production:
In the explosives industry, 2,4,6-Trinitrobenzoyl chloride is used as a key ingredient in the production of explosives and propellants. Its high reactivity and ability to form stable nitroaromatic compounds contribute to the effectiveness and performance of these products.
Used in Research and Development:
2,4,6-Trinitrobenzoyl chloride is also utilized in research and development settings for the study of its properties and potential applications. Its unique characteristics make it a valuable subject for scientific exploration and innovation in the field of chemistry.
Safety Precautions:
Due to its high toxicity and corrosive nature, 2,4,6-Trinitrobenzoyl chloride requires careful handling and storage. It is essential to follow safety protocols, such as wearing appropriate personal protective equipment, to minimize the risk of skin, eye, and respiratory system damage. Additionally, proper transportation and storage measures must be implemented to prevent accidental detonation and ensure the safety of those involved in its use.

InChI:InChI=1/C7H2ClN3O7/c8-7(12)6-4(10(15)16)1-3(9(13)14)2-5(6)11(17)18/h1-2H

Upstream product

• 129-66-8 2,4,6-trinitrobenzoic acid 
• 118-96-7 2,4,6-Trinitrotoluene 

Downstream Products

• 15012-38-1 methyl 2,4,6-trinitrobenzoate 
• 53848-88-7 2,4,6-trinitro-benzoic acid octyl ester 
• 2296-96-0 2,4,6-trinitro-benzoic acid ethyl ester 
• 51226-42-7 2,4,6-Trinitrobenzamide 
• 855272-80-9 2,4,6-trinitro-benzoyl azide 
• 374632-11-8 2,4,6-trinitro-benzoic acid p-toluidide 
• 321596-08-1 N-phenyl-2,4,6-trinitrobenzamide 
• 99057-40-6 2,4,6-trinitro-benzoic acid isopropyl ester 
• 321596-06-9 N-methyl-2,4,6-trinitrobenzamide 
• 33867-55-9 2,4,6-trinitro-benzoic acid benzyl ester 
• 53848-90-1 2,4,6-trinitro-benzoic acid butyl ester 

Relevant academic research and scientific papers

5,5′-Bis(2,4,6-trinitrophenyl)-2,2′-bi(1,3,4-oxadiazole) (TKX-55): Thermally Stable Explosive with Outstanding Properties

The novel, thermally stable explosive 5,5′-bis(2,4,6-trinitro-phenyl)-2,2′-bi(1,3,4-oxadiazole) (TKX-55) is reported. This compound can be prepared by means of a facile synthetic procedure and shows outstanding properties (detonation velocity, detonation pressure, sensitivity toward mechanical stimuli, and temperature of decomposition). TKX-55 was isolated and characterized by means of mass spectrometry, multinuclear (1H, 13C) NMR spectroscopy, and vibrational spectroscopy (IR and Raman). The structure in the crystalline state was determined by low-temperature single-crystal X-ray diffraction. From the calculated standard molar enthalpy of formation (CBS-4M) and the densities, the Chapman-Jouguet detonation properties were predicted by using the EXPLO5 V6.01 thermochemical computer code. The sensitivity of TKX-55 towards impact, friction, and electrostatic discharge was determined. The shock reactivity (explosiveness) of TKX-55 was measured by applying the small-scale shock reactivity test.

Synthetic utilization of polynitroaromatic compounds. 1. S-derivatization of 1-substituted 2,4,6-trinitrobenzenes with thiols

Reactions of 1-R-2,4,6-trinitrobenenes (R = alkyl, protected aldehyde, aminocarbonyl, cyano groups, or isoxazole ring) with thiol salts were investigated. In most cases, these reactions gave a mixture of minor para and major ortho substitution products. Reactions of N,N-disubstituted 2,4,6-trinitrobenzamides with S-,O-, and N-nucleophiles afforded products of substitution of the p-nitro group exclusively. 1-Cyano-2,4,6-trinitrobenzene was found to be the most reactive and the least selective: all three nitro groups can be substituted using an excess of thiol salts. 2-R-4,6-dinitrobenzamides showed no regioselectivity under similar conditions to yield 1:1 mixtures of para and ortho isomers.