34033-44-8

Usage

Uses

Used in Dye Production:
2,4-Dichloro-5-nitro-phenylamine is used as a chemical intermediate in the production of various dyes. Its unique structure and reactivity make it a valuable component in the synthesis of a wide range of dye compounds.
Used in Pharmaceutical Manufacturing:
DCNP is also utilized in the manufacturing of certain pharmaceuticals, where its specific chemical properties contribute to the development of drugs with targeted therapeutic effects.
Used in Research and Development:
Due to its potential mutagenic and genotoxic effects, DCNP is employed in research settings to study the mechanisms of genetic mutations and the development of cancer. This helps in understanding the risks associated with exposure to such compounds and contributes to the development of safer alternatives or mitigation strategies.

Upstream product

• 3698-83-7 2,4-dichloro-1,5-dinitrobenzene 
• 7664-93-9 sulfuric acid 
• 67-56-1 methanol 
• 7782-50-5 chlorine 
• 99-09-2 3-nitro-aniline 
• 554-00-7 2,4-Dichloroaniline 

Downstream Products

• 642068-49-3 2-bromo-4,6-dichloro-3-nitroaniline 
• 642068-48-2 1-bromo-3,5-dichloro-6-propylthio-2-nitrobenzene 
• 115423-89-7 1-bromo-3,5-dichloro-2,6-dinitrobenzene 

Relevant academic research and scientific papers

Design and syntheses of novel N -(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1 H -isoindole-1,3(2 H)-dione and N -(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors

Discovery of protoporphyrinogen oxidase (PPO, EC 1.3.3.4) inhibitors has been one of the hottest research areas in the field of herbicide development for many years. As a continuation of our research work on the development of new PPO-inhibiting herbicides, a series of novel N-(benzothiazol-5-yl)-4,5,6,7- tetrahydro-1H-isoindole-1,3(2H)-diones (1a-p) and N-(benzothiazol-5-yl) isoindoline-1,3-diones (2a-h) were designed and synthesized according to the ring-closing strategy of two ortho-substituents. The bioassay results indicated that some newly synthesized compounds exhibited higher PPO inhibition activity than the control of sulfentrazone. Compound 1a, S-(5-(1,3-dioxo-4,5,6,7- tetrahydro-1H-isoindol-2(3H)-yl)-6-fluorobenzothiazol-2-yl) O-methyl carbonothioate, was identified as the most potent inhibitor with ki value of 0.08 μM, about 9 times higher than that of sulfentrazone (k i = 0.72 μM). Further green house assay showed that compound 1b, methyl 2-((5-(1,3-dioxo-4,5,6,7-tetrahydro-1H-isoindol-2(3H)-yl)-6- fluorobenzothiazol-2-yl)thio)acetate, exhibited herbicidal activity comparable to that of sulfentrazone even at a concentration of 37.5 g ai/ha. In addition, among six tested crops, wheat exhibited high tolerance to compound 1b even at a dosage of 300 g ai/ha. These results indicated that compound 1b might have the potential to be developed as a new herbicide for weed control of wheat field.

Synthesis of Polyfunctionalized Biphenyls as Intermediates for a New Class of Liquid Crystals

A series of hexa- and octasubstituted biphenyls containing halogen, amino, nitro, and propylthio substituents were prepared by metal-mediated convergent synthesis from halobenzene precursors. The Pd-assisted C-C coupling methods were ineffective in the fo

1- (3-Heterocyclylphenyl) isothiourea, -isourea, -guanidine and -amidine herbicidal agents

There are provided 1-(3-heterocyclyphenyl)isothio-urea, -isourea, -guanidine and -amidine compounds of formula I Further provided are compositions and methods comprising those compounds for the control of undesirable plant species.

1-(3-Heterocyclylphenyl)isothiourea, -isourea, -guanidine and -amidine compounds as herbicides

There are provided 1-(3-heterocyclyphenyl)isothiourea, -isourea, -guanidine and -amidine compounds of formula I Further provided are compositions and methods comprising those compounds for the control of undesirable plant species.

Selective hydrogenation of polynitroaromatic derivatives with noble metal catalysts in the presence of catalytic amounts of iron

Hydrogen over PtO2, 5%Pd(c), PdCl2, or 5%Rh(al2O3), in the presence of catalytic amounts of iron and under mild reaction conditions, resulted in the selective reduction of a variety of polynitroaromatic compounds in high yields.