6264-73-9

Usage

Uses

Used in Dye Production:
2,4-Diaminodiphenyl ether is used as a precursor in the production of dyes, contributing to the synthesis of a wide range of colorants used in various industries.
Used in Polymer Synthesis:
In the polymer industry, 2,4-Diaminodiphenyl ether is utilized as a building block for creating polymers, which are essential in the manufacturing of plastics and other materials.
Used in Plastics Production:
2,4-Diaminodiphenyl ether is used as a key component in the production of certain types of plastics, enhancing their properties and expanding their applications.
Used in Pharmaceutical Industry:
As a precursor to certain pharmaceuticals, 2,4-Diaminodiphenyl ether plays a vital role in the development of drugs, showcasing its importance in the healthcare sector.
Overall, 2,4-Diaminodiphenyl ether's diverse applications across different industries underscore its value as a versatile and essential chemical compound.

Upstream product

• 7647-01-0 hydrogenchloride 
• 2486-07-9 2,4-dinitrophenyl phenyl ether 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 100-67-4 potassium phenolate 

Relevant academic research and scientific papers

Role of Alkali Halides in the Synthesis of Nitrogen Containing Heterocycles by Reductive Carbonylation of Aromatic Nitro-Derivatives Catalysed by Ru3(CO)12

The presence of alkali halides as co-catalysts in the reductive carbonylation of o-nitrobiphenyl 1 catalysed by Ru3(CO)12 strongly increases the rate of reactions and slectivity towards heterocyclization products .With sodium halides, depending on the anion, the selectivity for carbazole is in the order Cl- > Br- ca.F- I-; whereas the selectivity for 5H-phenanthridin-6-one is the reverse I- > Br- ca.F- > Cl-.The influence of the cation can be explained with the polarization of a CO ligand of the ruthenium cluster, due to the interaction of the alkali cation with the oxygen lone pair.In fact high yields (>80percent) of heterocyclization products are obtained when the alkali cation is free to coordinate the CO.When this interaction is reduced, by sequestering the cation with crown-ethers, or better with cryptands, the yield of heterocyclic products is 14percent and 0percent respectively.The role of the anion and cation in the catalytic mechanism are discussed.The attempted extension of this reaction to other nitro-derivatives for the potential synthesis of aromatic heterocycles with larger rings are also reported.