38411-17-5

Usage

Uses

Used in Pharmaceutical Industry:
N-(2,5-dichloro-4-nitrophenyl)acetamide is used as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicine.
Used in Agrochemical Industry:
N-(2,5-dichloro-4-nitrophenyl)acetamide is also used as an intermediate in the synthesis of agrochemicals. Its potential antibacterial and antifungal properties make it a valuable compound in the development of pesticides and other agricultural products, helping to improve crop yields and protect plants from diseases.
Used in Antibacterial Applications:
N-(2,5-dichloro-4-nitrophenyl)acetamide has been studied for its potential antibacterial properties. Its unique chemical structure allows it to target and inhibit the growth of bacteria, making it a promising candidate for the development of new antibacterial agents.
Used in Antifungal Applications:
Similarly, N-(2,5-dichloro-4-nitrophenyl)acetamide has been studied for its potential antifungal properties. Its ability to target and inhibit the growth of fungi makes it a valuable compound in the development of new antifungal agents, which can be used to treat various fungal infections.

Upstream product

• 2621-62-7 2,5-dichloroacetanilide 
• 7697-37-2 nitric acid 
• 6627-34-5 2,5-dichloro-4-nitroaniline 
• 75-36-5 acetyl chloride 

Downstream Products

• 6627-34-5 2,5-dichloro-4-nitroaniline 
• 781-15-7 1,2,3,4-tetrachloro-5,6-dinitrobenzene 
• 879-39-0 2,3,4,5-tetrachloronitrobenzene 
• 62406-69-3 2,3,6-trichloro-4-nitro-aniline 
• 17488-25-4 1,4-dichloro-2,5-dinitrobenzene 
• 97-50-7 5-chloro-2,4-dimethoxyaniline 
• 119-21-1 1-chloro-2,4-dimethoxy-5-nitrobenzene 
• 17801-99-9 1,4-dichloro-2-methoxy-5-nitrobenzene 
• 476660-79-4 dimethyl [5-(acetylamino)-4-chloro-2-nitrophenyl]malonate 
• 6392-96-7 2,5-dichloro-4-aminoacetanilide 

Relevant academic research and scientific papers

Variable noninnocence of substituted azobis(phenylcyanamido)diruthenium complexes

The synthetic chemistry of substituted 4,4′-azobis(phenylcyanamide) ligands was investigated, and the complexes [{Ru(tpy)(bpy)}2( μ-L)][PF6]2, where L = 2,2′:5,5′-tetramethyl-4,4′-azobis(phenylcyanamido) (Me4adpc2-), 2,2′-dimethyl-4,4′-azobis(phenylcyanamido) (Me2adpc2-), unsubstituted (adpc2-), 3,3′-dichloro-4,4′-azobis(phenylcyanamido) (Cl2adpc2-), and 2,2′:5,5′-tetrachloro-4,4′-azobis(phenylcyanamido) (Cl4adpc2-), were prepared and characterized by cyclic voltammetry and vis-near-IR (NIR) and IR spectroelectrochemistry. The room temperature electron paramagnetic resonance spectrum of [{Ru(tpy)(bpy)}2( μ-Me4adpc)]3+ showed an organic radical signal and is consistent with an oxidation-state description [RuII, Me4adpc?-, RuII]3+, while that of [{Ru(tpy)(bpy)}2( μ-Cl2adpc)]3+ at 10 K showed a low-symmetry RuIII signal, which is consistent with the description [RuIII, Cl2adpc2-, RuII]3+. IR spectroelectrochemistry data suggest that [{Ru(tpy)(bpy)}2( μ-adpc)]3+ is delocalized and [{Ru(tpy)(bpy)}2( μ-Cl2adpc)]3+ and [{Ru(tpy)(bpy)}2( μ-Cl4adpc)]3+ are valence-trapped mixed-valence systems. A NIR absorption band that is unique to all [{Ru(tpy)(bpy)}2( μ-L)]3+ complexes is observed; however, its energy and intensity vary depending on the nature of the bridging ligand and, hence, the complexes oxidation-state description.

Construction of interconnected acidity functions based on ortho substituted anilines and N-methylanilines as indicators

The log I values of 15 mainly ortho substituted derivatives of aniline and N-methylaniline have been measured spectrophotometrically in sulfuric, perchloric, and methanesulfonic acids. A new algorithm has been suggested for construction of acidity functions enabling simultaneous and independent construction of acidity functions in various media under the condition of equal values of pKa of the same indicators in the given media. The so-called interconnected acidity functions have been constructed with using this algorithm and the log I values measured in the above media, and the pKa values have been calculated. The resulting acidity functions and pKa values agree well with the corresponding literature data.